510(k) Report

510(k) · Cleared

Cleared

T2 Alpha Femur Retrograde Nailing System, T2 Alpha Femur Antegrade GT/PF Nailing System, T2 Tibial Nailing System, T2 Femoral System, T2 Supracondylar Nail System

K203819510(k) TraditionalCleared Feb 26, 202159-day reviewClass II21 CFR 888.3020

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

Stryker GmbH · HSB Rod, Fixation, Intramedullary And Accessories

Cleared on Feb 26, 2021 as substantially equivalent to K200880 (Stryker GmbH, 2020) and 2 other predicates after a 59-day review. Its family tree reaches back 8 generations to 1997. 7 later devices descend from it.

Decided
Feb 26, 2021
Review
59 days
Class
Class II
Product code
HSB
Recalls
None
Predicates
3

Its longest line of descent runs back 8 generations to K970097 (1997). 53 ancestors in all, the oldest K871539 (1987). 7 later devices descend from it, 3 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2020: 1 other ancestor2010: 3 other ancestors2013: 2 other ancestors2008: 2 other ancestors2005: 4 other ancestors2003: 4 other ancestors2002: 4 other ancestors2001: 6 other ancestors2000: 1 other ancestor1996: 2 other ancestors1993: 1 other ancestor2011: 1 other ancestor2004: 4 other ancestors1987: 1 other ancestor2006: 1 other ancestor1998: 3 other ancestors1997: 2 other ancestors1992: 1 other ancestor1999: 1 other ancestor1995: 1 other ancestor2025: 2 descendants cleared2023: 1 descendant cleared2022: 2 descendants cleared2026: 2 descendants clearedK970097 · Proximal Femoral Nail (PFN) System · Synthes (Usa) · 1997K973240 · Synthes Proximal Femoral Nail (PFN) System Modification · Synthes (Usa) · 1997K013563 · Long Trochanteric Nail System · DePuy Orthopaedics, Inc. · 2001 · recalledK033329 · Depuy Ace Universal and Troch Entry Femoral Nail Systems · Depuy, Inc. · 2003K083497 · Zimmer Natural Nail System Piriformis Fossa and Greater Trochanter Antegrade Femoral Nails · Zimmer, Inc. · 2009 · recalled×2: 2 generations cleared close together, K172774 (2018), K180436 (2018) K191271 · T2 Alpha Femur Antegrade GT/PF Nailing System, T2 Alpha Tibia Nailing System, IMN Screws System, IMN Instruments System · Stryker Trauma GmbH · 20191990200020102020
  1. Root · 8 generations backK970097 Proximal Femoral Nail (PFN) SystemSynthes (Usa) · 1997
  2. 7 generations backK973240 Synthes Proximal Femoral Nail (PFN) System ModificationSynthes (Usa) · 1997
  3. 6 generations backK013563 Long Trochanteric Nail SystemDePuy Orthopaedics, Inc. · 2001 · Recalled
  4. 5 generations backK033329 Depuy Ace Universal and Troch Entry Femoral Nail SystemsDepuy, Inc. · 2003
  5. 4 generations backK083497 Zimmer Natural Nail System Piriformis Fossa and Greater Trochanter…Zimmer, Inc. · 2009 · Recalled
  6. 3 generations backK172774 T2 Alpha Femur Antegrade GT/PF Nailing System, IMN Screws System…Stryker Trauma GmbH · 2018
  7. 2 generations backK180436 T2 Alpha Tibia Nailing System, T2 Alpha Femur Antegrade GT/PF…Stryker Trauma GmbH · 2018
  8. 1 generation backK191271 T2 Alpha Femur Antegrade GT/PF Nailing System, T2 Alpha Tibia…Stryker Trauma GmbH · 2019
  9. This deviceK203819 T2 Alpha Femur Retrograde Nailing System, T2 Alpha Femur Antegrade…Stryker GmbH · 2021
  10. Descendant · cites it directly · 3 of its ownK213328 Gamma4 System, Gamma3 System, IMN Screws System, T2 Tibial Nailing…Stryker GmbH · 2022 · Recalled
  11. Descendant · cites it directly · 2 of its ownK250163 T2 Alpha Femur Retrograde Nailing SystemStryker GmbH · 2025
  12. Descendant · 2 generations on · 1 of its ownK253640 T2 Alpha Femur Retrograde Nailing System; Pangea Femur…Stryker GmbH · 2026
  13. Descendant · 3 generations on · 0 of its ownK261481 Pangea Femur Reconstruction SystemStryker GmbH · 2026
  14. Descendant · 2 generations on · 0 of its ownK251400 T2 Alpha Humerus Nailing System; IMN Screws System; T2 Nailing SystemStryker GmbH · 2025

Showing 5 of 7 descendants. See all descendants

Descendants cleared per year

2022: 22023: 12025: 22026: 2
2022high 2 (2022) · low 0 (2024)2026

Most influential descendants

Showing 5 of 7 · See all
  • K213328Gamma4 System, Gamma3 System, IMN Screws System, T2 Tibial Nailing SystemStryker GmbH · 2022 · cites it directly3descendants
  • K250163T2 Alpha Femur Retrograde Nailing SystemStryker GmbH · 2025 · cites it directly2descendants
  • K253640T2 Alpha Femur Retrograde Nailing System; Pangea Femur Reconstruction SystemStryker GmbH · 2026 · 2 generations on1descendant
  • K261481Pangea Femur Reconstruction SystemStryker GmbH · 2026 · 3 generations on0descendants
  • K251400T2 Alpha Humerus Nailing System; IMN Screws System; T2 Nailing SystemStryker GmbH · 2025 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K970097Proximal Femoral Nail (PFN) SystemSynthes (Usa)1997—
−7K973240Synthes Proximal Femoral Nail (PFN) System ModificationSynthes (Usa)1997—
−6K013563Long Trochanteric Nail SystemDePuy Orthopaedics, Inc.200154
−5K033329Depuy Ace Universal and Troch Entry Femoral Nail SystemsDepuy, Inc.2003—
−4K083497Zimmer Natural Nail System Piriformis Fossa and Greater Trochanter Antegrade…Zimmer, Inc.200916
−3K172774T2 Alpha Femur Antegrade GT/PF Nailing System, IMN Screws System, IMN…Stryker Trauma GmbH2018—
−2K180436T2 Alpha Tibia Nailing System, T2 Alpha Femur Antegrade GT/PF Nailing System…Stryker Trauma GmbH2018—
−1K191271T2 Alpha Femur Antegrade GT/PF Nailing System, T2 Alpha Tibia Nailing System…Stryker Trauma GmbH2019—
0 (this device)K203819T2 Alpha Femur Retrograde Nailing System, T2 Alpha Femur Antegrade GT/PF…Stryker GmbH2021—
+1K213328Gamma4 System, Gamma3 System, IMN Screws System, T2 Tibial Nailing SystemStryker GmbH20221
+1K250163T2 Alpha Femur Retrograde Nailing SystemStryker GmbH2025—
+2K253640T2 Alpha Femur Retrograde Nailing System; Pangea Femur Reconstruction SystemStryker GmbH2026—
+3K261481Pangea Femur Reconstruction SystemStryker GmbH2026—
+2K251400T2 Alpha Humerus Nailing System; IMN Screws System; T2 Nailing SystemStryker GmbH2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198710
199210
199310
199510
199620
199720
199830
199910
200010
200160
200240
200340
200440
200540
200610
200820
201030
201110
201320
202010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202220
202310
202520
202620
FIG. 1 — Lineage of K203819, 1997–2026Source: 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? (3)

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
*K200880T2 Tibial Nailing System, T2 Femoral Nail System, T2 Supracondylar Nail System, T2 Recon…
Summary page 9
…ation, intramedullary and accessories) Regulatory Class: Class II III. PREDICATE DEVICE Primary Predicate: T2 Supracondylar Nail System (K200880) Additional Predicates: T2 Femoral Nail (K200880) Zimmer Natural Nail System Retrograd…
Stryker GmbH2020—
*K101622Zimmer Natural Nail System Retrograde Femoral Nails
Summary page 9
…al Predicates: T2 Femoral Nail (K200880) Zimmer Natural Nail System Retrograde Femoral Nails (K101622) T2 GTN (K200880) T2 Tibial Nailing System (K200880)…
Zimmer, Inc.20103
*K191271T2 Alpha Femur Antegrade GT/PF Nailing System, T2 Alpha Tibia Nailing System, IMN Screws…
Summary page 9
…T2 Tibial Nailing System (K200880) T2 Alpha Femur Antegrade GT/PF Nailing System (K191271) K203819…
Stryker Trauma GmbH2019—

Also cleared against K200880: 2 other devices →

What descends from it? (7)

3 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K213328Gamma4 System, Gamma3 System, IMN Screws System, T2 Tibial Nailing SystemStryker GmbH20223
K250163T2 Alpha Femur Retrograde Nailing SystemStryker GmbH20252
K230512Gamma4 SystemStryker GmbH20230

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

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 24 years and passes through 6 companies; a new generation was cleared every 1.9 years on median.
  • 29 of the 53 ancestors have a recall of any class.
  • Of its descendants, K213328 (Stryker GmbH, 2022) has gone furthest, with 3 descendants of its own.
  • 2 other devices also cite its predicate K200880.

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. 2021, 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?

The indications for use of this internal fixation device include: • Open and closed femoral fractures • Pseudoarthrosis and correction osteotomy • Pathologic fractures, impending pathologic fractures, and tumor resections • Supracondylar fractures, including those with intra-articular extension • Fractures involving osteopenic and osteoporotic bone • Fractures distal to a total hip prosthesis • Periprosthetic fractures • Nonunions and malunions The…

Read the full statement (425 words)

The indications for use of this internal fixation device include:

• Open and closed femoral fractures

• Pseudoarthrosis and correction osteotomy

• Pathologic fractures, impending pathologic fractures, and tumor resections

• Supracondylar fractures, including those with intra-articular extension

• Fractures involving osteopenic and osteoporotic bone

• Fractures distal to a total hip prosthesis

• Periprosthetic fractures

• Nonunions and malunions

The indications for use of these internal fixation devices include:

- Fixation of subtrochanteric, intertrochanteric, ipsilateral neck/shaft, comminuted proximal femoral shaft fractures

- Femoral fixation required as a result of pathological disease

- Temporary stabilization of fractures of the femoral shaft ranging from the femoral neck to the supracondylar regions of the femur

- Open and closed femoral fractures

- Pseudoarthrosis and correction osteotomy

- Pathologic fractures, impending pathologic fractures and tumor resections

- Ipsilateral femur fractures

- Fractures proximal to a total knee arthroplasty

- Nonunions and malunions

- Fractures involving osteopenic and osteoporotic bone

The Compression Screw Femur may also be used in conjunction with the T2 Alpha Femur Retrograde System.

The T2 Tibial Nailing System is intended to provide temporary stabilization of various types of fractures, malunions and nonunion of the tibia. The nails are inserted using an opened or closed technique and can be statically, dynamically and compressed locked.

The T2 Tibial Nailing System is indicated for long bone fracture fixation, specifically tibial fracture fixation, which may include the following:

• Open and closed tibial fractures

• Pseudoarthrosis and correction osteotomy

• Pathologic fractures, impending pathologic fractures, and tumor resections

• Nonunion and malunion

The Locking Screws may also be used in conjunction with the T2 Alpha Systems.

The T2 Femoral Nail is indicated for long bone fracture fixation specifically femoral fracture fixation which may include the following:

• Open and closed femoral fractures

• Pseudoarthrosis and correction osteotomy

• Pathologic fractures, impending pathologic fractures, and tumor resections

• Supracondylar fractures, including those with intra-articular extension

• Ipsilateral femur fractures

• Fractures proximal to a total knee arthroplasty

• Fractures distal to hip joint

• Nonunions and malunions

The Condyle Nut and Condyle Screws may also be used in conjunction with the T2 Alpha Femur Retrograde System.

The T2 Supracondylar Nail System is indicated for:

• Open and closed femoral fractures

• Pseudoarthrosis and correction osteotomy

• Pathologic fractures, impending pathologic fractures, and tumor resections

• Supracondylar fractures including those with intra-articular extension

• Fractures distal to a total hip prosthesis

• Nonunions and malunions

The End Cap may also be used in conjunction with the T2 Alpha Femur Retrograde System.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K203819: T2 Alpha Femur Retrograde Nailing System, T2 Alpha Femur Antegrade GT/PF Nailing System, T2 Tibial Nailing System, T2 Femoral System, T2 Supracondylar Nail System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K203819

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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