510(k) Report

510(k) · Cleared

Cleared

Depuy Orthotech Spiked Washer

K983906510(k) TraditionalCleared Dec 18, 199845-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 Orthopaedics, Inc. · HTN Washer, Bolt Nut

Cleared on Dec 18, 1998 as substantially equivalent to K961649 (Smith & Nephew Endoscopy, Inc., 1996) and 1 other predicate after a 45-day review. Its family tree reaches back 2 generations to 1987.

Decided
Dec 18, 1998
Review
45 days
Class
Class II
Product code
HTN
Recalls
None
Predicates
2

Its longest line of descent runs back 2 generations to K871037 (1987). 3 ancestors in all. No later device cites it as a predicate yet.

Other ancestors, by year cleared 1991: 1 other ancestorK871037 · Cancellous Fixation Screw & Washer for Use W/Screw · Concept, Inc. · 1987K961649 · Acufex Tibial Anchor Screw & Spiked Washer · Smith & Nephew Endoscopy, Inc. · 19961985199019952000
  1. Root · 2 generations backK871037 Cancellous Fixation Screw & Washer for Use W/ScrewConcept, Inc. · 1987
  2. 1 generation backK961649 Acufex Tibial Anchor Screw & Spiked WasherSmith & Nephew Endoscopy, Inc. · 1996
  3. This deviceK983906 Depuy Orthotech Spiked WasherDePuy Orthopaedics, Inc. · 1998
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K871037Cancellous Fixation Screw & Washer for Use W/ScrewConcept, Inc.1987—
−1K961649Acufex Tibial Anchor Screw & Spiked WasherSmith & Nephew Endoscopy, Inc.1996—
0 (this device)K983906Depuy Orthotech Spiked WasherDePuy Orthopaedics, Inc.1998—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199110
FIG. 1 — Lineage of K983906, 1987–1998Source: 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 HTN? 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 HTN device

  1. #1 K201522 Arthrex Syndesmosis TightRope XP Buttress…score 16.5 · 6 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
*K961649Acufex Tibial Anchor Screw & Spiked Washer
Summary page 1
…bone fixation appliances and accessories DEVICE PRODUCT CODE: 87HTN, HWC SUBSTANTIALLY EQUIVALENT DEVICES: Smith-Nephew Acufex® Tibial Anchor Screw & Spiked Washer (K961649) Synthes® Spiked Washer (K914472) DEVICE DESCRIPTION AND INTENDED USE: The DePuy OrthoTech Spiked Washer is a circular device w…
Smith & Nephew Endoscopy, Inc.1996—
*K914472Spiked Washer
Summary page 1
…essories DEVICE PRODUCT CODE: 87HTN, HWC SUBSTANTIALLY EQUIVALENT DEVICES: Smith-Nephew Acufex® Tibial Anchor Screw & Spiked Washer (K961649) Synthes® Spiked Washer (K914472) DEVICE DESCRIPTION AND INTENDED USE: The DePuy OrthoTech Spiked Washer is a circular device with eight inferior (fixative surf…
Synthes (Usa)1991—

Also cleared against K961649: 1 other device →

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 11 years and passes through 3 companies; a new generation was cleared every 9.3 years on median.
  • None of the 3 ancestors has a recall.
  • 1 other device also cites its predicate K961649.

How does its category compare?

All HTN devices

HTN Washer, Bolt Nut: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · HTN

4in 2025

2007: 12008: 22009: 32011: 42013: 32014: 82015: 22016: 12017: 62018: 22019: 52020: 32021: 22022: 52023: 22024: 62025: 42026 (partial year): 2
2007high 8 (2014) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HTN

75in 2025

2009: 86 days median2011: 130 days median2013: 105 days median2014: 98 days median2017: 88 days median2019: 116 days median2020: 87 days median2022: 86 days median2024: 90 days median2025: 75 days median
2007high 130 (2011) · low 75 (2025)2026

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

Recalls per year · HTN

1in 2019

2013: 12019: 1
2007high 1 (2013) · low 0 (2007)2026

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

Adverse event reports per year · HTN

190in 2025

2007: 142008: 112009: 222010: 172011: 122012: 692013: 452014: 332015: 352016: 432017: 302018: 482019: 532020: 812021: 1492022: 852023: 1082024: 2692025: 190
2007high 269 (2024) · low 11 (2008)2025

MAUDE reports naming product code HTN, 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
20071—014
20082—011
2009386022
20100—017
20114130012
20120—069
20133105145
2014898033
20152—035
20161—043
2017688030
20182—048
20195116153
2020387081
20212—0149
2022586085
20232—0108
20246900269
20254750190
20262—0—

What is it indicated for?

The DePuy OrthoTech Spiked Washer is intended for use with a 6.5mm cancellous thread or a 4.5mm cortical thread low profile head screw for fixation of soft tissue, such as tendon and ligaments, to bone in orthopaedic procedures.

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. “K983906: Depuy Orthotech Spiked Washer.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K983906

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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