510(k) Report

510(k) · Cleared

Cleared

TriMed Clavicle Fixation System

K230805510(k) TraditionalCleared Sep 1, 2023162-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

TriMed, Inc. · HRS Plate, Fixation, Bone

Cleared on Sep 1, 2023 as substantially equivalent to K112509 (TriMed, Inc., 2011) and 1 other predicate after a 162-day review. Its family tree reaches back 10 generations to 1996.

Decided
Sep 1, 2023
Review
162 days
Class
Class II
Product code
HRS
Recalls
None
Predicates
2

Its longest line of descent runs back 10 generations to K962616 (1996). 36 ancestors in all, the oldest K890939 (1989). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2020: 1 other ancestor2011: 1 other ancestor2001: 4 other ancestors2000: 5 other ancestors2010: 1 other ancestor2007: 1 other ancestor2005: 1 other ancestor1995: 1 other ancestor1991: 1 other ancestor1989: 1 other ancestor2003: 1 other ancestor2004: 3 other ancestors1999: 2 other ancestors1998: 2 other ancestors1996: 1 other ancestorK962616 · 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. · 2006K100944 · Clavicle Locking Plate System · Newclip Technics · 2010K112509 · Trimed Clavicle Fixation System · TriMed, Inc. · 20111990200020102020
  1. Root · 10 generations backK962616 Synthes Dorsal Distal Radius Plate (DDRP) SystemSynthes (Usa) · 1996
  2. 6 generations between
  3. 3 generations backK061352 Peri-Loc Periarticular Locked Plating System for the Upper ExtremitySmith & Nephew, Inc. · 2006
  4. 2 generations backK100944 Clavicle Locking Plate SystemNewclip Technics · 2010
  5. 1 generation backK112509 Trimed Clavicle Fixation SystemTriMed, Inc. · 2011
  6. This deviceK230805 TriMed Clavicle Fixation SystemTriMed, Inc. · 2023
Show all 10 generations
  1. Root · 10 generations backK962616 Synthes Dorsal Distal Radius Plate (DDRP) SystemSynthes (Usa) · 1996
  2. 9 generations backK982732 Synthes (Usa) Distal Radius Plate System (DRPS)Synthes · 1998
  3. 8 generations backK023007 Distal Radius Fracture Repair SystemHand Innovations, Inc. · 2002
  4. 7 generations backK030198 Hand Innovations, Inc. Distal Radius Fracture Repair SystemHand Innovations, Inc. · 2003
  5. 6 generations backK032705 Distal Radius Fracture Repair SystemHand Innovations, Inc. · 2003
  6. 5 generations backK050932 Distal Volar Radius Anatomical Plate SystemHand Innovations, Inc. · 2005 · Recalled
  7. 4 generations backK051735 Peri-Loc Locking Bone Plates and Locking Bone Screws for the Upper…Smith & Nephew, Inc. · 2005
  8. 3 generations backK061352 Peri-Loc Periarticular Locked Plating System for the Upper ExtremitySmith & Nephew, Inc. · 2006
  9. 2 generations backK100944 Clavicle Locking Plate SystemNewclip Technics · 2010
  10. 1 generation backK112509 Trimed Clavicle Fixation SystemTriMed, Inc. · 2011
  11. This deviceK230805 TriMed Clavicle Fixation SystemTriMed, Inc. · 2023
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−10K962616Synthes Dorsal Distal Radius Plate (DDRP) SystemSynthes (Usa)1996—
−9K982732Synthes (Usa) Distal Radius Plate System (DRPS)Synthes1998—
−8K023007Distal Radius Fracture Repair SystemHand Innovations, Inc.2002—
−7K030198Hand Innovations, Inc. Distal Radius Fracture Repair SystemHand Innovations, Inc.2003—
−6K032705Distal Radius Fracture Repair SystemHand Innovations, Inc.2003—
−5K050932Distal Volar Radius Anatomical Plate SystemHand Innovations, Inc.20051
−4K051735Peri-Loc Locking Bone Plates and Locking Bone Screws for the Upper ExtremitySmith & Nephew, Inc.2005—
−3K061352Peri-Loc Periarticular Locked Plating System for the Upper ExtremitySmith & Nephew, Inc.2006—
−2K100944Clavicle Locking Plate SystemNewclip Technics2010—
−1K112509Trimed Clavicle Fixation SystemTriMed, Inc.2011—
0 (this device)K230805TriMed Clavicle Fixation SystemTriMed, Inc.2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198910
199110
199510
199610
199820
199920
200050
200140
200310
200430
200510
200710
201010
201110
202010
FIG. 1 — Lineage of K230805, 1996–2023Source: 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
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What was it cleared against? (2)

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
*K112509Trimed Clavicle Fixation System
Summary page 4
…Product Codes: HRS (Primary), HWC (a)(3). Predicate Device: Primary Predicate Device K112509 – TriMed Clavicle Fixation System, TriMed, Inc. (USA)…
TriMed, Inc.2011—
*K201321DePuy Synthes 2.7mm VA LCP Clavicle Plate System
Summary page 4
…Med, Inc. (USA) Additional Predicate Device K201321 – DePuy Synthes 2.7mm VA LCP Clavicle Plate System (CHE) (a)(4). Device Description…
DePuy Synthes20201

What descends from it?

No later submission names this one as a predicate yet.

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 27 years and passes through 6 companies; a new generation was cleared every 1.6 years on median.
  • 9 of the 36 ancestors have a recall of any class.

How does its category compare?

All HRS devices

HRS Plate, Fixation, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, 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 TriMed Clavicle Fixation Plates and Screws are indicated for use in fixation of fractures, malunions, non-unions, and osteotomies of the clavicle.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K230805: TriMed Clavicle Fixation System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K230805

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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