510(k) Report

510(k) · Cleared

Cleared

Synthes Locking Hand Plates

K092247510(k) TraditionalCleared Sep 25, 200959-day reviewClass II21 CFR 888.3030

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

Synthes (Usa) · HRS Plate, Fixation, Bone

Cleared on Sep 25, 2009 after a 59-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 28 later devices descend from it.

Decided
Sep 25, 2009
Review
59 days
Class
Class II
Product code
HRS
Recalls
None
Predicates
0

28 later devices descend from it, 8 citing it directly.

Descendants, by year cleared 2022: 1 descendant cleared2014: 1 descendant cleared2026: 7 descendants cleared2017: 3 descendants cleared2024: 6 descendants cleared2015: 1 descendant cleared2019: 1 descendant cleared2023: 3 descendants cleared2020: 1 descendant cleared2018: 1 descendant cleared2025: 3 descendants cleared20052010201520202025
  1. This deviceK092247 Synthes Locking Hand PlatesSynthes (Usa) · 2009
  2. Descendant · cites it directly · 8 of its ownK213864 Bonebridge Osteosynthesis Plating SystemBonebridge AG · 2022
  3. Descendant · 2 generations on · 7 of its ownK231292 TAMINA 3.5mm Proximal Humerus System; POYA 3.5MM Lateral Proximal…Bonebridge AG · 2023
  4. Descendant · cites it directly · 7 of its ownK141527 Depuy Synthes Variable Angle Locking Hand SystemSynthes USA · 2015
  5. Descendant · 3 generations on · 4 of its ownK240318 SITTER 3.5mm Versatile SystemBonebridge AG · 2024
  6. Descendant · cites it directly · 4 of its ownK233665 DePuy Synthes VOLT Mini Fragment Plating System, DePuy Synthes VOLT…DePuy Synthes · 2024

Showing 5 of 28 descendants. See all descendants

Descendants cleared per year

2014: 12015: 12017: 32018: 12019: 12020: 12022: 12023: 32024: 62025: 32026: 7
2014high 7 (2026) · low 0 (2016)2026

Most influential descendants

Showing 5 of 28 · See all
  • K213864Bonebridge Osteosynthesis Plating SystemBonebridge AG · 2022 · cites it directly8descendants
  • K231292TAMINA 3.5mm Proximal Humerus System; POYA 3.5MM Lateral Proximal Tibia System; LORRAINE…Bonebridge AG · 2023 · 2 generations on7descendants
  • K141527Depuy Synthes Variable Angle Locking Hand SystemSynthes USA · 2015 · cites it directly7descendants
  • K240318SITTER 3.5mm Versatile SystemBonebridge AG · 2024 · 3 generations on4descendants
  • K233665DePuy Synthes VOLT Mini Fragment Plating System, DePuy Synthes VOLT Small Fragment…DePuy Synthes · 2024 · cites it directly4descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K092247Synthes Locking Hand PlatesSynthes (Usa)2009—
+1K213864Bonebridge Osteosynthesis Plating SystemBonebridge AG2022—
+2K231292TAMINA 3.5mm Proximal Humerus System; POYA 3.5MM Lateral Proximal Tibia…Bonebridge AG2023—
+1K141527Depuy Synthes Variable Angle Locking Hand SystemSynthes USA2015—
+3K240318SITTER 3.5mm Versatile SystemBonebridge AG2024—
+1K233665DePuy Synthes VOLT Mini Fragment Plating System, DePuy Synthes VOLT Small…DePuy Synthes2024—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201410
201510
201730
201810
201910
202010
202210
202330
202460
202530
202670
FIG. 1 — Lineage of K092247, 2009–2026Source: 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 510(k) statement (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?

FDA’s file for it is a 510(k) statement, which names no predicate.

What descends from it? (28)

See all 28

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

NumberDeviceApplicantDecidedDescendants
K213864Bonebridge Osteosynthesis Plating SystemBonebridge AG20228
K141527Depuy Synthes Variable Angle Locking Hand SystemSynthes USA20157
K233665DePuy Synthes VOLT Mini Fragment Plating System, DePuy Synthes VOLT Small Fragment…DePuy Synthes20244
K170705ARIX Wrist SystemJeil Medical Corporation20172
K142418I.T.S. Hand Locking Plates System - HLSI.T.S. GmbH20141
K254162KLS Martin Ixos SystemKLS Martin L.P.20260
K191972ARIX Wrist SystemJeil Medical Corporation20190
K160553DePuy Synthes 4.0 mm and 5.0 mm Locking Screws – MR Conditional, DePuy Synthes Wrist…Synthes (Usa) Products, LLC / Depuy Orthopaedics, Inc.20170

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?

  • Of its descendants, K213864 (Bonebridge AG, 2022) has gone furthest, with 8 descendants of its own.

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 Synthes Locking Hand Plates are intended for fixation of fractures. osteotomies, non-unions, replantations and fusions of small bones and small bone fragments, particularly in osteopenic bone.

Indications for use as stated in the FDA 510(k) statement.

Cite this page

510(k) Report. “K092247: Synthes Locking Hand Plates.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K092247

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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