510(k) Report

510(k) · Cleared

Recalled · Class II · 2019

Smith & Nephew, Inc. Intramedullary Nail System Instrumentation

K122170510(k) TraditionalCleared Oct 19, 201288-day reviewClass II21 CFR 888.3020Recalls 1

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Smith & Nephew, Inc. · HSB Rod, Fixation, Intramedullary And Accessories

Cleared on Oct 19, 2012 as substantially equivalent to K811002 (Richard'S Medical Equip., Inc., 1981) and 17 other predicates after an 88-day review. Its family tree reaches back 5 generations to 1998. It has been recalled once.

Decided
Oct 19, 2012
Review
88 days
Class
Class II
Product code
HSB
Recalls
1
Predicates
18

Its longest line of descent runs back 5 generations to K981529 (1998). 35 ancestors in all, the oldest K811002 (1981). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2011: 1 other ancestor2006: 2 other ancestors2005: 2 other ancestors2004: 3 other ancestors2003: 4 other ancestors2002: 1 other ancestor1998: 3 other ancestors1996: 1 other ancestor1981: 1 other ancestor2001: 3 other ancestors1999: 2 other ancestors1995: 5 other ancestors1989: 1 other ancestor1992: 1 other ancestorK981529 · Titanium Intramedullary Nail, Titanium Locking Screw · Smith & Nephew, Inc. · 1998 · recalled×2: 2 generations cleared close together, K040212 (2004), K040656 (2004) K050226 · Asian Intramedullary Hip Screw Nails · Smith & Nephew, Inc. · 2005K092748 · Sureshot Tan Nails and Accessories · Smith & Nephew, Inc. · 2010 · recalled1980198519901995200020052010
  1. Root · 5 generations backK981529 Titanium Intramedullary Nail, Titanium Locking ScrewSmith & Nephew, Inc. · 1998 · Recalled
  2. 4 generations backK040212 Trigen IntertanSmith & Nephew, Inc. · 2004 · Recalled
  3. 3 generations backK040656 Modification to Smith & Nephew Intramedullary Hip ScrewSmith & Nephew, Inc. · 2004
  4. 2 generations backK050226 Asian Intramedullary Hip Screw NailsSmith & Nephew, Inc. · 2005
  5. 1 generation backK092748 Sureshot Tan Nails and AccessoriesSmith & Nephew, Inc. · 2010 · Recalled
  6. This deviceK122170 Smith & Nephew, Inc. Intramedullary Nail System InstrumentationSmith & Nephew, Inc. · 2012
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K981529Titanium Intramedullary Nail, Titanium Locking ScrewSmith & Nephew, Inc.19982
−4K040212Trigen IntertanSmith & Nephew, Inc.20046
−3K040656Modification to Smith & Nephew Intramedullary Hip ScrewSmith & Nephew, Inc.2004—
−2K050226Asian Intramedullary Hip Screw NailsSmith & Nephew, Inc.2005—
−1K092748Sureshot Tan Nails and AccessoriesSmith & Nephew, Inc.20101
0 (this device)K122170Smith & Nephew, Inc. Intramedullary Nail System InstrumentationSmith & Nephew, Inc.2012—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198110
198910
199210
199550
199610
199830
199920
200130
200210
200340
200430
200520
200620
201110
FIG. 1 — Lineage of K122170, 1998–2012Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in HSB? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new HSB device

  1. #1 K200869 Gamma3 Systemscore 19.8 · 8 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (18)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K811002Ender Pins
Summary page 1
…ponent metallic bone fixation appliances and accessories Device Class: Class II Panel Code: Orthopaedics/87 Predicate Devices: Ender Nail (K811002); TriMax Nail System (K964163); Friedi Gliding Nail modified (K974409); Titanium Nail System (K9…
Richard'S Medical Equip., Inc.1981—
*K964163Trimax Nail System
Summary page 1
…and accessories Device Class: Class II Panel Code: Orthopaedics/87 Predicate Devices: Ender Nail (K811002); TriMax Nail System (K964163); Friedi Gliding Nail modified (K974409); Titanium Nail System (K981529); Friedi Gliding Nails a…
Smith & Nephew Richards, Inc.1996—
*K974409Friedl Gliding Nail System
Summary page 1
…I Panel Code: Orthopaedics/87 Predicate Devices: Ender Nail (K811002); TriMax Nail System (K964163); Friedi Gliding Nail modified (K974409); Titanium Nail System (K981529); Friedi Gliding Nails addition smaller nails (K020240); IP-XS C…
Plus Orthopedics1998—
*K981529Titanium Intramedullary Nail, Titanium Locking Screw
Summary page 1
…te Devices: Ender Nail (K811002); TriMax Nail System (K964163); Friedi Gliding Nail modified (K974409); Titanium Nail System (K981529); Friedi Gliding Nails addition smaller nails (K020240); IP-XS Compression Nail System (K032548);…
Smith & Nephew, Inc.19982
*K020240Slim Gliding Nail System
Summary page 1
…l System (K964163); Friedi Gliding Nail modified (K974409); Titanium Nail System (K981529); Friedi Gliding Nails addition smaller nails (K020240); IP-XS Compression Nail System (K032548); TriGen Straight Humeral Nail System (K032722); Friedl…
Plus Orthopedics20021
*K032548IP-XS Compression Nail System
Summary page 1
…odified (K974409); Titanium Nail System (K981529); Friedi Gliding Nails addition smaller nails (K020240); IP-XS Compression Nail System (K032548); TriGen Straight Humeral Nail System (K032722); Friedl Gliding Nails Gliding nails with chamfered blade (K…
Plus Orthopedics2003—
*K032722Trigen Straight Humeral Nail System
Summary page 1
…9); Friedi Gliding Nails addition smaller nails (K020240); IP-XS Compression Nail System (K032548); TriGen Straight Humeral Nail System (K032722); Friedl Gliding Nails Gliding nails with chamfered blade (K033763) TriGen InterTAN Nail (K040212)…
Smith & Nephew, Inc.2003—
*K033763Modification to Slim Gliding Nail System
Summary page 1
…IP-XS Compression Nail System (K032548); TriGen Straight Humeral Nail System (K032722); Friedl Gliding Nails Gliding nails with chamfered blade (K033763) TriGen InterTAN Nail (K040212) TriGen 1300 TAN Nails (K(040462); Intramedullary Hip Screw (K(04…
Plus Orthopedics2003—
*K040212Trigen Intertan
Summary page 1
…; TriGen Straight Humeral Nail System (K032722); Friedl Gliding Nails Gliding nails with chamfered blade (K033763) TriGen InterTAN Nail (K040212) TriGen 1300 TAN Nails (K(040462); Intramedullary Hip Screw (K(040656); TriGen Adolescent TAN (K…
Smith & Nephew, Inc.20046
*K040462Trigen Trochanteric Antegrade Nail
Summary page 1
…tem (K032722); Friedl Gliding Nails Gliding nails with chamfered blade (K033763) TriGen InterTAN Nail (K040212) TriGen 1300 TAN Nails (K(040462); Intramedullary Hip Screw (K(040656); TriGen Adolescent TAN (K(040929) TriGen Hindfoot Fusion N…
Smith & Nephew, Inc.20042
*K040656Modification to Smith & Nephew Intramedullary Hip Screw
Summary page 1
…liding nails with chamfered blade (K033763) TriGen InterTAN Nail (K040212) TriGen 1300 TAN Nails (K(040462); Intramedullary Hip Screw (K(040656); TriGen Adolescent TAN (K(040929) TriGen Hindfoot Fusion Nail (HFN) (K(043052); Titanium Knee F…
Smith & Nephew, Inc.2004—
*K040929Trigen Adolescent Tan
Summary page 1
…TriGen InterTAN Nail (K040212) TriGen 1300 TAN Nails (K(040462); Intramedullary Hip Screw (K(040656); TriGen Adolescent TAN (K(040929) TriGen Hindfoot Fusion Nail (HFN) (K(043052); Titanium Knee Fusion Nail (1(050938); TriGen Meta…
Smith & Nephew, Inc.2004—
*K043052Trigen Hindfoot Fusion Nail
Summary page 1
…en 1300 TAN Nails (K(040462); Intramedullary Hip Screw (K(040656); TriGen Adolescent TAN (K(040929) TriGen Hindfoot Fusion Nail (HFN) (K(043052); Titanium Knee Fusion Nail (1(050938); TriGen Meta-Nail Retrograde Femoral and Tibial Nails (K(061019);…
Smith & Nephew, Inc.20047
*K050938Knee Fusion Nail
Summary page 1
…ullary Hip Screw (K(040656); TriGen Adolescent TAN (K(040929) TriGen Hindfoot Fusion Nail (HFN) (K(043052); Titanium Knee Fusion Nail (1(050938); TriGen Meta-Nail Retrograde Femoral and Tibial Nails (K(061019); TriGen Stainless Steel Knee Fusion Nails…
Smith & Nephew, Inc.2005—
*K061019Trigen Meta-Nail Retrograde Femoral and Tibial Nails
Summary page 1
…TriGen Hindfoot Fusion Nail (HFN) (K(043052); Titanium Knee Fusion Nail (1(050938); TriGen Meta-Nail Retrograde Femoral and Tibial Nails (K(061019); TriGen Stainless Steel Knee Fusion Nails (K(061783); SURESHOT TAN Nails and Accessories (K(092748);…
Smith & Nephew, Inc.20061
*K061783Knee Fusion Nail
Summary page 1
…Titanium Knee Fusion Nail (1(050938); TriGen Meta-Nail Retrograde Femoral and Tibial Nails (K(061019); TriGen Stainless Steel Knee Fusion Nails (K(061783); SURESHOT TAN Nails and Accessories (K(092748); 4.5mm and 5.0mm TriGen Low Profile Bone Screw (1(111025);…
Smith & Nephew, Inc.2006—
*K092748Sureshot Tan Nails and Accessories
Summary page 1
…eta-Nail Retrograde Femoral and Tibial Nails (K(061019); TriGen Stainless Steel Knee Fusion Nails (K(061783); SURESHOT TAN Nails and Accessories (K(092748); 4.5mm and 5.0mm TriGen Low Profile Bone Screw (1(111025); Device Description Subject of this Traditional 510(…
Smith & Nephew, Inc.20101
*K111025Trigen Low Profile Bone Screw
Summary page 1
…riGen Stainless Steel Knee Fusion Nails (K(061783); SURESHOT TAN Nails and Accessories (K(092748); 4.5mm and 5.0mm TriGen Low Profile Bone Screw (1(111025); Device Description Subject of this Traditional 510(k) Premarket Notification are the Smith & Nephew, Inc. Intramedull…
Smith & Nephew, Inc.20111

Also cleared against K811002: 2 other devices →

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Oct 7, 2019Class IIZ-0351-2020Process controlLAG SCREW 3.2 GUIDE PIN SLEEVE are being recalled due to a manufacturing error. The detent balls in the guide pin sleeve were not drilled to the correct depth, which will cause them to not fully compress.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 14 years and passes through 1 company; a new generation was cleared every 2.5 years on median.
  • 13 of the 35 ancestors have a recall of any class.
  • 2 other devices also cite its predicate K811002.

How does its category compare?

All HSB devices

HSB Rod, Fixation, Intramedullary And Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · HSB

15in 2025

2007: 82008: 112009: 182010: 142011: 162012: 172013: 182014: 192015: 222016: 82017: 232018: 172019: 132020: 172021: 102022: 122023: 112024: 132025: 152026 (partial year): 18
2007high 23 (2017) · low 8 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HSB

106in 2025

2007: 68 days median2008: 57 days median2009: 86 days median2010: 117 days median2011: 78 days median2012: 112 days median2013: 105 days median2014: 147 days median2015: 111 days median2016: 124 days median2017: 119 days median2018: 134 days median2019: 132 days median2020: 112 days median2021: 94 days median2022: 172 days median2023: 162 days median2024: 195 days median2025: 106 days median2026 (partial year): 151 days median
2007high 195 (2024) · low 57 (2008)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · HSB

18in 2025

2008: 92009: 812010: 182011: 22012: 72013: 142014: 32015: 32016: 62017: 662018: 562019: 62020: 62021: 22022: 12023: 12024: 12025: 182026 (partial year): 1
2007high 81 (2009) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · HSB

2,911in 2025

2007: 1622008: 1842009: 3342010: 4542011: 6622012: 1,0792013: 1,7732014: 1,4742015: 1,6712016: 1,9202017: 1,4472018: 3,5262019: 2,5172020: 3,2992021: 4,1112022: 2,7332023: 2,2192024: 2,8692025: 2,911
2007high 4,111 (2021) · low 162 (2007)2025

MAUDE reports naming product code HSB, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20078680162
200811579184
2009188681334
20101411718454
201116782662
20121711271,079
201318105141,773
20141914731,474
20152211131,671
2016812461,920
201723119661,447
201817134563,526
20191313262,517
20201711263,299
2021109424,111
20221217212,733
20231116212,219
20241319512,869
202515106182,911
2026181511—

What is it indicated for?

Smith & Nephew Trigen Adolescent TAN Nail System and Trigen 1300 TAN Nail System Instruments are accessory devices and are intended to be used to assist in the implantation of the Smith & Nephew Trigen Adolescent TAN Nail System and the Smith & Nephew Trigen 1300 TAN Nail System and their cleared indications for use. Indications for interlocking intramedullary nails include: * Simple long bone fractures * Severely comminuted, spiral, large oblique and…

Read the full statement (1,844 words)

Smith & Nephew Trigen Adolescent TAN Nail System and Trigen 1300 TAN Nail System Instruments are accessory devices and are intended to be used to assist in the implantation of the Smith & Nephew Trigen Adolescent TAN Nail System and the Smith & Nephew Trigen 1300 TAN Nail System and their cleared indications for use.

Indications for interlocking intramedullary nails include:

* Simple long bone fractures

* Severely comminuted, spiral, large oblique and segmental fractures

* Nonunions and malunions

* Poly trauma and multiple fractures

* Prophylactic nailing of impending pathologic fractures

* Reconstruction following tumor resection and grafting

* Supracondylar fractures

* Bone lengthening and shortening

* Fractures that occur in and between the proximal and distal third of the long bones being treated

In addition to the indications for interlocking intramedullary nails, devices that contain holes/slots proximally to accept screws that thread into the femoral head for compression and rotational stability are indicated for the following:

* Subtrochanteric fractures with lesser trochanteric involvement

* Ipsilateral femoral shaft/neck fractures

* Intertrochanteric fractures

Smith & Nephew Trigen Nail System Instruments are accessory devices and are intended to be used to assist in the implantation of Smith & Nephew Trigen System and its cleared indications for use.

TRIGEN 0 Humeral Nail System is indicated for:

* Proximal and/or diaphyseal fractures of the humerus

* Nonunions

* Malalignments

* Pathological humeral fractures

* Impending pathological fractures

Smith & Nephew Trigen InterTAN Nail System Instruments are accessory devices and are intended to be used to assist in the implantation of Smith & Nephew Trigen InterTAN Nail System and its cleared indications for use.

TRIGEN InterTAN Nails are indicated for:

* Simple long bone fractures

* Severely comminuted spiral, long oblique, and segmental shaft

* Nonunions and malunions

* Poly trauma and multiple fractures

* Prophylactic nailing of impending pathologic fractures

* Reconstruction, following tumor resection and grafting

* Bone lengthening and shortening

* Subtrochanteric fractures

* Ipsilateral femoral shaft/neck fractures

* Intertrochanteric fractures

* Intracapsular fractures

Smith & Nephew Intramedullary Nail Systems Instruments are accessory devices and are intended to be used to assist in the implantation of Smith & Nephew Intramedullary Nail Systems and their cleared indications for use.

The Short Knee Nail, REVISION 0 Nail and Hindfoot Fusion Nail (HFN) are indicated for:

* Degeneration, deformity, or trauma of both the tibiotalar and talocalcaneal articulations of the hindfoot

* Tibiocalcaneal arthrodesis

* Combined arthrodesis of the ankle and sub-talar joints

* Avascular necrosis of the ankle and sub-talar joints

* Failed total ankle replacement with sub-talar intrusion

* Failed ankle arthrodesis with insufficient talar body

* Rheumatoid arthritis

* Severe deformity secondary to untreated talipes eguinovarus or neuromuscular disease

* Severe pilon fractures with trauma to the subtalar joint

Smith & Nephew SURESHOT TAN Nail Systems Instruments are accessory devices and are intended to be used to assist in the implantation of Smith & Nephew SURESHOT TAN Nail Systems and their cleared indications for use.

SURESHOT TAN Nails are indicated for:

* Fractures of the femur including:

o simple long bone fractures

o severely comminuted, spiral, large oblique and segmental fractures

* Non unions and malunions

* Poly trauma and multiple fractures

* Prophylactic nailing of impending pathologic fractures

* Reconstruction, following tumor resection and grafting

* Supracondylar fractures

* Bone lengthening and shortening

* Fixation of fractures that occur in and between the proximal third and distal fourth of the femur

In addition, SURESHOT TAN Nails contain holes/slots proximally to accept screws that thread into the femoral head for compression and rotational stability and are indicated for the following:

* Subtrochanteric fractures;

* Intertrochanteric fractures;

* Ipsilateral femoral shaft/neck fractures;

* Intracapsular fractures.

Smith & Nephew Intramedullary Hip Screw System Instruments are accessory devices and are intended to be used to assist in the implantation of Smith & Nephew Intramedullary Hip Screw Systems and their cleared indications for use.

Intramedullary Hip Screws are indicated for:

* Intracapsular fractures of the femoral neck;

* Trochanteric or subtrochanteric fractures;

* Osteotomies for patients with diseases or deformities of the hip;

* Hip arthrodesis;

* Supracondylar fractures and distal femoral fractures using a supracondylar plate;

* Ipsilateral femoral shaft/neck fractures;

* Intertrochanteric fractures;

* Femoral neck fractures;

* Subrapital fractures;

* Comminuted neck and shaft fractures;

* Femur reconstruction following tumor resection;

* Leg length discrepancies secondary to femoral inequality;

* Prophylactic nailing of impending pathologic fractures.

Smith & Nephew Ender Nail System Instruments are accessory devices and are intended to be used to assist in the implantation of Smith & Nephew Ender Nail Systems and their cleared indications for use.

ENDER Nails are indicated for:

* Fracture of the neck, trochanteric, and subtrochanteric region of the femur;

* Distal femoral fractures with a distal fragment 10cm or longer

* Tibial shaft fractures

* Proximal humeral fractures

Smith & Nephew TriMax Nail System Instruments are accessory devices and are intended to be used to assist in the implantation of Smith & Nephew TriMax Nail Systems and their cleared indications for use.

Femoral/Recon antegrade nails and retrograde nails are indicated for:

* Shaft fractures including severely comminuted, spiral, large oblique and segmental fractures

* Non-unions and malunions

* Bone lengthening/shortening

* Severely comminuted shaft fractures

* Pathologic fractures, pseudloarthrosis, failed osteosynthesis

* Closed supracondylar fractures

* Prophylactic nailing of impeding pathologic fractures

Additional indications for the femoral/recon antegrade include:

* Subtrochanteric fractures with lesser trochanteric involvement

* Ipsilateral femoral shaft/neck fractures

Additional indications for retrograde nails include:

* Severely comminuted supracondylar fractures with or without difficult intra-articular extension

* Fractures that require opening the knee joint to stabilize the femoral condylar segment

* Fractures above total knee implants

The TriMax Nail System is intended to be removed upon fracture healing.

Indications for interlocking intramedullary nails include:

* Simple long bone fractures

* Severely comminuted, spiral, large oblique and segmental fractures

* Nonunions and malunions

* Poly trauma and multiple fractures

* Prophylactic nailing of impending pathologic fractures

* Reconstruction following tumor resection and grafting

* Supracondylar fractures

* Bone lengthening and shortening

* Fractures that occur in and between the proximal and distal third of the long bones being treated

In addition to the indications for interlocking intramedullary nails, devices that contain holes/slots proximally to accept screws that thread into the femoral head for compression and rotational stability (e.g. Femoral Antegrade Nail, Trochanteric Antegrade Nail and Femoral/Recon Antegrade Nail) are indicated for the following:

* Subtrochanteric fractures

* Intertrochanteric fractures

* Ipsilateral femoral shaft/neck fractures

In addition to the indications for interlocking intramedullary nails, devices that use a retrograde femoral surgical approach (e.g. Knee Nail, Retrograde and Supracondylar Nails) are indicated for:

* Comminuted supracondylar fractures with or without intra-articular extension

* Fractures that require opening the knee joint to stabilize the femoral condylar segment

* Fractures above total knee implants (peri-prosthetic fractures)

Smith & Nephew Knee Fusion Nail Instruments are accessory devices and are intended to be used to assist in the implantation of Smith & Nephew Knee Fusion Nails and their cleared indications for use.

Knee Fusion Nails are indicated for:

* Intramedullary Knee Arthrodesis

Smith & Nephew IP-XS Compression Nail System Instruments are accessory devices and are intended to be used to assist in the implantation of the Smith & Nephew IP-XS Compression Nail System and its cleared indications for use.

The IP-XS Compression Nail System is inserted into the medullary canal of long bones for the:

* Alignment, stabilization, and fixation of fractures caused by disease or trauma

* The fixation of long bones that have been surgically prepared (osteotomy) for correction of deformity

* Arthrodesis

Smith & Nephew SLIM (Friedi) Gliding Nail Systems Instruments are accessory devices and are intended to be used to assist in the implantation of Smith & Nephew SLIM (Friedi) Gliding Nails and their cleared indications for use.

The SLIM (Friedl) Gliding Nail System is an all-purpose locking nail system for ensuring primary load stability in:

* Petrochanteric femoral fractures

* Subtrochanteric femoral fractures

* Lateral femoral neck fractures

Internal fixation with the SLIM (Friedl) Gliding Nail System is indicated in all combination injuries involving the lateral femoral neck or trochanter region and femoral shaft fractures. Thanks to its biomechanical characteristics, the SLIM (Friedl) Gliding Nail System is also suitable for medical femoral neck fractures with retention of the head and simple femoral shaft fractures down to the distal metaphysis. Gliding nail fixation can also be used to secure pathological fractures or to provide weight-bearing stability after varus and valgus revision osteotomies of the proximal femur.

Smith & Nephew TriGen Low Profile Bone Screw Instruments are accessory devices and are intended to be used to assist in the implantation of Smith & Nephew TriGen Low Profile Bone Screws and their cleared indications for use.

The TRIGEN TM Low Profile Bone Screw can be used with several types of nails in Smith & Nephew's (TRIGEN TM) Titanium Nail System. The TRIGEN TM Low Profile Bone Screw therefore has the following indications:

Indications for interlocking intramedullary nails include simple long bone fractures; severely comminuted, spiral, large oblique and segmental fractures; nonunions and malunions; polytrauma and multiple fractures; prophylactic nailing of impending pathologic fractures; reconstruction following tumor resection and grafting; supracondylar fractures; bone lengthening and shortening. Interlocking intramedullary nails are indicated for fixation of fractures that occur in and between the proximal and distal third of the long bones being treated.

In addition to the indications for interlocking intramedullary nails, devices that contain holes/slots proximally to accept screws that thread into the femoral head for compression and rotational stability (e.g. Femoral Antegrade Nail, Trochanteric Antegrade Nail and Femoral/Recon Antegrade Nail) are indicated for the following: subtrochanteric fractures, intertrochanteric fractures, and ipsilateral femoral shaft/neck fractures.

In addition to the indications for interlocking intramedullary nails, devices that use a retrograde femoral surgical approach (e.g. Knee Nail, Retrograde and Supracondylar Nails) are indicated for the following: comminuted supracondylar fractures with or without intra-articular extension; fractures that require opening the knee joint to stabilize the femoral condylar segment; fractures above total knee implants (peri-prosthetic fractures).

The TRIGEN TM InterTAN nails are indicated for fractures of the femur including: simple shaft fractures, comminuted shaft fractures, spiral shaft fractures, long oblique shaft fractures and segmental shaft fractures; subtrochanteric fractures; intertrochanteric fractures; ipsilateral femoral shaft/neck fractures; intracapsular fractures; nonunions and malunions; polytrauma and multiple fractures; prophylactic nailing of impending pathologic fractures; reconstruction, following tumor resection and grafting; bone lengthening and shortening.

SURESHOT TM TAN Nails are indicated for fractures of the femur including simple long bone fractures, severely comminuted, spiral, large oblique and segmental fractures; nonunions and malunions; polytrauma and multiple fractures; prophylactic nailing of impending pathologic fractures; reconstruction, following tumor resection and grafting; supracondylar fractures; bone lengthening and shortening; and for fixation of fractures that occur in and between the proximal third and distal fourth of the femur.

In addition, SURESHOT TM TAN Nails contain holes/slots proximally to accept screws that thread into the femoral head for compression and rotational stability and are indicated for the following: subtrochanteric fractures; intertrochanteric fractures; ipsilateral femoral shaft/neck fractures; and intracapsular fractures.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K122170: Smith & Nephew, Inc. Intramedullary Nail System Instrumentation.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K122170

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026