510(k) Report

510(k) · Cleared

Cleared

Depuy Motech Peak 3MM Fixation Rod System

K980368510(k) TraditionalCleared Apr 14, 199874-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

Depuy, Inc. · HRS Plate, Fixation, Bone

Cleared on Apr 14, 1998 after a 74-day review. The FDA summary names its predicate without a number. 11 later devices descend from it.

Decided
Apr 14, 1998
Review
74 days
Class
Class II
Product code
HRS
Recalls
None
Predicates
0

11 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 2019: 1 descendant cleared1998: 1 descendant cleared2020: 4 descendants cleared2021: 1 descendant cleared2026: 3 descendants cleared2023: 1 descendant cleared1995200020052010201520202025
  1. This deviceK980368 Depuy Motech Peak 3MM Fixation Rod SystemDepuy, Inc. · 1998
  2. Descendant · cites it directly · 10 of its ownK982483 Depuy Motech Peak Fixation SystemDePuy Orthopaedics, Inc. · 1998
  3. Descendant · cites it directly · 9 of its ownK190895 MOUNTAINEER OCT Spinal System, SUMMIT SI OCT Spinal Fixation System…Medos International SARL · 2019
  4. Descendant · 2 generations on · 3 of its ownK200936 Invictus™ CT Spinal Fixation SystemAlphatec Spine, Inc. · 2020
  5. Descendant · 2 generations on · 3 of its ownK192014 SYPMHONY™ OCT SystemMedos International SARL · 2020
  6. Descendant · 2 generations on · 2 of its ownK192646 SYMPHONY™ OCT SystemMedos International SARL · 2020

Showing 5 of 11 descendants. See all descendants

Descendants cleared per year

1998: 12019: 12020: 42021: 12023: 12026: 3
1998high 4 (2020) · low 0 (1999)2026

Most influential descendants

Showing 5 of 11 · See all
  • K982483Depuy Motech Peak Fixation SystemDePuy Orthopaedics, Inc. · 1998 · cites it directly10descendants
  • K190895MOUNTAINEER OCT Spinal System, SUMMIT SI OCT Spinal Fixation System, SYMPHONY OCT…Medos International SARL · 2019 · cites it directly9descendants
  • K200936Invictus™ CT Spinal Fixation SystemAlphatec Spine, Inc. · 2020 · 2 generations on3descendants
  • K192014SYPMHONY™ OCT SystemMedos International SARL · 2020 · 2 generations on3descendants
  • K192646SYMPHONY™ OCT SystemMedos International SARL · 2020 · 2 generations on2descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K980368Depuy Motech Peak 3MM Fixation Rod SystemDepuy, Inc.1998—
+1K982483Depuy Motech Peak Fixation SystemDePuy Orthopaedics, Inc.1998—
+1K190895MOUNTAINEER OCT Spinal System, SUMMIT SI OCT Spinal Fixation System, SYMPHONY…Medos International SARL2019—
+2K200936Invictus™ CT Spinal Fixation SystemAlphatec Spine, Inc.2020—
+2K192014SYPMHONY™ OCT SystemMedos International SARL2020—
+2K192646SYMPHONY™ OCT SystemMedos International SARL2020—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199810
201910
202040
202110
202310
202630
FIG. 1 — Lineage of K980368, 1998–2026Source: 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
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What was it cleared against? (1)

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
*—ACE 3.5 mm Reconstruction Plate
Named without a submission number
—

What descends from it? (11)

See all 11

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

NumberDeviceApplicantDecidedDescendants
K982483Depuy Motech Peak Fixation SystemDePuy Orthopaedics, Inc.199810
K190895MOUNTAINEER OCT Spinal System, SUMMIT SI OCT Spinal Fixation System, SYMPHONY OCT…Medos International SARL20199

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, K982483 (DePuy Orthopaedics, Inc., 1998) has gone furthest, with 10 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.

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 DePuy Motech PEAK 3mm Fixation Rod System is intended for use in treating fractures of the pelvis, acetabulum, clavicle, scapula, and distal humerus.

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. “K980368: Depuy Motech Peak 3MM Fixation Rod System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K980368

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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