510(k) Report

510(k) · Cleared

Recalled · Class II · 2017

Peri-Loc Periarticular Locked Plating System

K092015510(k) SpecialCleared Jul 30, 200924-day reviewClass II21 CFR 888.3030Recalls 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. · HRS Plate, Fixation, Bone

Cleared on Jul 30, 2009 as substantially equivalent to K033669 (Smith & Nephew, Inc., 2003) and 2 other predicates after a 24-day review. Its family tree reaches back 8 generations to 1996. 41 later devices descend from it. It has been recalled once.

Decided
Jul 30, 2009
Review
24 days
Class
Class II
Product code
HRS
Recalls
1
Predicates
3

Its longest line of descent runs back 8 generations to K962616 (1996). 29 ancestors in all, the oldest K890939 (1989). 41 later devices descend from it, 9 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2003: 1 other ancestor2004: 3 other ancestors2001: 4 other ancestors2000: 5 other ancestors1999: 2 other ancestors1998: 2 other ancestors1995: 1 other ancestor1991: 1 other ancestor1989: 1 other ancestor1996: 1 other ancestor2020: 2 descendants cleared2025: 8 descendants cleared2022: 4 descendants cleared2017: 2 descendants cleared2021: 3 descendants cleared2010: 1 descendant cleared2013: 2 descendants cleared2026: 4 descendants cleared2014: 1 descendant cleared2016: 1 descendant cleared2018: 3 descendants cleared2023: 3 descendants cleared2024: 7 descendants clearedK962616 · Synthes Dorsal Distal Radius Plate (DDRP) System · Synthes (Usa) · 1996K982732 · Synthes (Usa) Distal Radius Plate System (DRPS) · Synthes · 1998×2: 2 generations cleared close together, K023007 (2002), K030198 (2003) K032705 · Distal Radius Fracture Repair System · Hand Innovations, Inc. · 2003×2: 2 generations cleared close together, K050932 (2005), K051735 (2005) K061352 · Peri-Loc Periarticular Locked Plating System for the Upper Extremity · Smith & Nephew, Inc. · 20061990200020102020
  1. Root · 8 generations backK962616 Synthes Dorsal Distal Radius Plate (DDRP) SystemSynthes (Usa) · 1996
  2. 7 generations backK982732 Synthes (Usa) Distal Radius Plate System (DRPS)Synthes · 1998
  3. 6 generations backK023007 Distal Radius Fracture Repair SystemHand Innovations, Inc. · 2002
  4. 5 generations backK030198 Hand Innovations, Inc. Distal Radius Fracture Repair SystemHand Innovations, Inc. · 2003
  5. 4 generations backK032705 Distal Radius Fracture Repair SystemHand Innovations, Inc. · 2003
  6. 3 generations backK050932 Distal Volar Radius Anatomical Plate SystemHand Innovations, Inc. · 2005 · Recalled
  7. 2 generations backK051735 Peri-Loc Locking Bone Plates and Locking Bone Screws for the Upper…Smith & Nephew, Inc. · 2005
  8. 1 generation backK061352 Peri-Loc Periarticular Locked Plating System for the Upper ExtremitySmith & Nephew, Inc. · 2006
  9. This deviceK092015 Peri-Loc Periarticular Locked Plating SystemSmith & Nephew, Inc. · 2009
  10. Descendant · cites it directly · 33 of its ownK123055 Smith & Nephew, Inc Screw and Plate System InstrumentationSmith & Nephew, Inc. · 2013
  11. Descendant · 2 generations on · 32 of its ownK140814 Evos Mini-Fragment Plating SystemSmith & Nephew, Inc. · 2014 · Recalled
  12. Descendant · 3 generations on · 14 of its ownK163361 ANTHEM™ Fracture SystemGlobus Medical, Inc. · 2017
  13. Descendant · cites it directly · 11 of its ownK173166 ANTHEM Fracture SystemGlobus Medical, Inc. · 2017
  14. Descendant · 2 generations on · 10 of its ownK180554 ANTHEM Fracture SystemGlobus Medical, Inc. · 2018

Showing 5 of 41 descendants. See all descendants

Descendants cleared per year

2010: 12013: 22014: 12016: 12017: 22018: 32020: 22021: 32022: 42023: 32024: 72025: 82026: 4
2010high 8 (2025) · low 0 (2011)2026

Most influential descendants

Showing 5 of 41 · See all
  • K123055Smith & Nephew, Inc Screw and Plate System InstrumentationSmith & Nephew, Inc. · 2013 · cites it directly33descendants
  • K140814Evos Mini-Fragment Plating SystemSmith & Nephew, Inc. · 2014 · 2 generations on32descendants
  • K163361ANTHEM™ Fracture SystemGlobus Medical, Inc. · 2017 · 3 generations on14descendants
  • K173166ANTHEM Fracture SystemGlobus Medical, Inc. · 2017 · cites it directly11descendants
  • K180554ANTHEM Fracture SystemGlobus Medical, Inc. · 2018 · 2 generations on10descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K962616Synthes Dorsal Distal Radius Plate (DDRP) SystemSynthes (Usa)1996—
−7K982732Synthes (Usa) Distal Radius Plate System (DRPS)Synthes1998—
−6K023007Distal Radius Fracture Repair SystemHand Innovations, Inc.2002—
−5K030198Hand Innovations, Inc. Distal Radius Fracture Repair SystemHand Innovations, Inc.2003—
−4K032705Distal Radius Fracture Repair SystemHand Innovations, Inc.2003—
−3K050932Distal Volar Radius Anatomical Plate SystemHand Innovations, Inc.20051
−2K051735Peri-Loc Locking Bone Plates and Locking Bone Screws for the Upper ExtremitySmith & Nephew, Inc.2005—
−1K061352Peri-Loc Periarticular Locked Plating System for the Upper ExtremitySmith & Nephew, Inc.2006—
0 (this device)K092015Peri-Loc Periarticular Locked Plating SystemSmith & Nephew, Inc.2009—
+1K123055Smith & Nephew, Inc Screw and Plate System InstrumentationSmith & Nephew, Inc.2013—
+2K140814Evos Mini-Fragment Plating SystemSmith & Nephew, Inc.20142
+3K163361ANTHEM™ Fracture SystemGlobus Medical, Inc.2017—
+1K173166ANTHEM Fracture SystemGlobus Medical, Inc.2017—
+2K180554ANTHEM Fracture SystemGlobus Medical, Inc.2018—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198910
199110
199510
199610
199820
199920
200050
200140
200310
200430

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201010
201320
201410
201610
201720
201830
202020
202130
202240
202330
202470
202580
202640
FIG. 1 — Lineage of K092015, 1996–2026Source: 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 HRS? 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 HRS device

  1. #1 K222465 Tyber Medical Anatomical Plating Systemscore 27.5 · 16 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
*K033669Smith & Nephew Locking Bone Plate System (Locking Bone Plates and Screws)
Summary page 1
…/ Orthopedics I 87 Device Description: The subject devices are design modifications to PERI-LOC TM Periarticular Locked Plating System devices previously cleared under K033669, K051735 and K061352. Like the predicate devices listed below, the subject components include various sizes of contoured, locking…
Smith & Nephew, Inc.20031
*K051735Peri-Loc Locking Bone Plates and Locking Bone Screws for the Upper Extremity
Summary page 1
…edics I 87 Device Description: The subject devices are design modifications to PERI-LOC TM Periarticular Locked Plating System devices previously cleared under K033669, K051735 and K061352. Like the predicate devices listed below, the subject components include various sizes of contoured, locking bone pla…
Smith & Nephew, Inc.2005—
*K061352Peri-Loc Periarticular Locked Plating System for the Upper Extremity
Summary page 1
…Device Description: The subject devices are design modifications to PERI-LOC TM Periarticular Locked Plating System devices previously cleared under K033669, K051735 and K061352. Like the predicate devices listed below, the subject components include various sizes of contoured, locking bone plates made fro…
Smith & Nephew, Inc.2006—

Also cleared against K033669: 27 other devices →

What descends from it? (41)

See all 41

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

NumberDeviceApplicantDecidedDescendants
K123055Smith & Nephew, Inc Screw and Plate System InstrumentationSmith & Nephew, Inc.201333
K173166ANTHEM Fracture SystemGlobus Medical, Inc.201711
K210837Smith & Nephew Plates and ScrewsSmith & Nephew, Inc.20217
K201918EVOS Large Fragment Plating SystemSmith & Nephew, Inc.20204
K203405EVOS Large Fragment Plating SystemSmith & Nephew, Inc.20213
K213126Smith & Nephew, Inc. Plates and Screws Systems: EVOS, Peri-Loc, D-Rad, TC-100, VLP…Smith & Nephew, Inc.20222
K130810Zimmer Motionloc Screw for Periarticular Locking Plate SystemZimmer, Inc.20131
K093868I.T.S. LRS Locking Reconstruction SystemI.T.S. Implantat-Technologie-Systeme GmbH20101
K242973CanMINI Hand and Foot SystemCanwell Medical Co., Ltd.20250

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

Recalls of this device

DateClassRecallRoot causeReason
Mar 22, 2017Class IIZ-2036-2017Mixed-up of materials/componentsThis lot of left plates were laser etched and packaged as right plates.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 13 years and passes through 4 companies; a new generation was cleared every 1.6 years on median.
  • 7 of the 29 ancestors have a recall of any class.
  • Of its descendants, K123055 (Smith & Nephew, Inc., 2013) has gone furthest, with 33 descendants of its own.
  • 27 other devices also cite its predicate K033669.

How does its category compare?

All HRS devices

HRS Plate, Fixation, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years. 2009, this device’s year, is highlighted.

FDA decisions per year · HRS

54in 2025

2007: 352008: 352009: 472010: 492011: 432012: 592013: 562014: 762015: 562016: 442017: 572018: 402019: 462020: 482021: 402022: 472023: 402024: 542025: 542026 (partial year): 51
2007high 76 (2014) · low 35 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HRS

90in 2025

2007: 63 days median2008: 87 days median2009: 85 days median2010: 100 days median2011: 88 days median2012: 106 days median2013: 89 days median2014: 57 days median2015: 97 days median2016: 109 days median2017: 122 days median2018: 116 days median2019: 89 days median2020: 88 days median2021: 87 days median2022: 144 days median2023: 120 days median2024: 96 days median2025: 90 days median2026 (partial year): 82 days median
2007high 144 (2022) · low 57 (2014)2026

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

Recalls per year · HRS

1in 2025

2007: 22008: 112009: 32010: 162011: 52012: 42013: 112015: 72016: 52017: 32018: 22019: 252020: 12021: 92022: 32023: 12025: 12026 (partial year): 3
2007high 25 (2019) · low 0 (2014)2026

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

Adverse event reports per year · HRS

2,306in 2025

2007: 3392008: 3112009: 4352010: 4912011: 7732012: 1,6632013: 2,6432014: 2,4132015: 3,0952016: 2,2762017: 2,2202018: 2,6632019: 3,3592020: 2,7902021: 2,4422022: 1,7002023: 2,0492024: 1,8492025: 2,306
2007high 3,359 (2019) · low 311 (2008)2025

MAUDE reports naming product code HRS, 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
200735632339
2008358711311
200947853435
20104910016491
201143885773
20125910641,663
20135689112,643
2014765702,413
2015569773,095
20164410952,276
20175712232,220
20184011622,663
20194689253,359
2020488812,790
2021408792,442
20224714431,700
20234012012,049
2024549601,849
2025549012,306
202651823—

What is it indicated for?

The PERI-LOC TM Periarticular Locked Plating System can be used for adult and pediatric patients, as well as patients with osteopenic bone. PERI-LOCTM bone plates and screws are indicated for fixation of pelvic, small and long bone fractures, including those of the tibia, fibula, femur, pelvis, acetabulum, metacarpals, metatarsals, humerus, ulna, radius, calcaneus, and clavicle.

Components in the PERI-LOC TM Periarticular Locked Plating System are for single use only.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K092015: Peri-Loc Periarticular Locked Plating System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K092015

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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