510(k) Report

510(k) · Cleared

Cleared

Profile Femoral Hip Prosthesis W/Porocoat

K872776510(k) TraditionalCleared Aug 24, 198741-day reviewClass II21 CFR 888.3360

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

Depuy, Inc. · KWL Prosthesis, Hip, Hemi-, Femoral, Metal

Cleared on Aug 24, 1987 after a 41-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Aug 24, 1987
Review
41 days
Class
Class II
Product code
KWL
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 1999: 1 descendant cleared1990200020102020
  1. This deviceK872776 Profile Femoral Hip Prosthesis W/PorocoatDepuy, Inc. · 1987
  2. Descendant · cites it directly · 0 of its ownK984459 Depuy Profile Femoral Hip with PorocoatDePuy Orthopaedics, Inc. · 1999

Most influential descendants

Showing 1 of 1 · See all
  • K984459Depuy Profile Femoral Hip with PorocoatDePuy Orthopaedics, Inc. · 1999 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K872776Profile Femoral Hip Prosthesis W/PorocoatDepuy, Inc.1987—
+1K984459Depuy Profile Femoral Hip with PorocoatDePuy Orthopaedics, Inc.1999—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199910
FIG. 1 — Lineage of K872776, 1987–1999Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in KWL? 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 KWL device

  1. #1 K253675 OsteoRemedies Hip Spacer Systemscore 16.0 · 9 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?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K984459Depuy Profile Femoral Hip with PorocoatDePuy Orthopaedics, Inc.19990

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, K984459 (DePuy Orthopaedics, Inc., 1999) has gone furthest, with 0 descendants of its own.

How does its category compare?

All KWL devices

KWL Prosthesis, Hip, Hemi-, Femoral, Metal: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · KWL

3in 2025

2007: 22008: 12011: 22012: 12015: 12018: 22019: 12020: 12022: 12024: 12025: 32026 (partial year): 2
2007high 3 (2025) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KWL

32in 2025

2025: 32 days median
2007high 32 (2025)2026

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

Recalls per year · KWL

2in 2017

2007: 362009: 22015: 12017: 22026 (partial year): 1
2007high 36 (2007) · low 0 (2008)2026

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

Adverse event reports per year · KWL

29in 2025

2007: 112008: 132009: 212010: 552011: 512012: 622013: 892014: 1072015: 2232016: 2102017: 3472018: 2942019: 4152020: 2702021: 1072022: 992023: 482024: 1432025: 29
2007high 415 (2019) · low 11 (2007)2025

MAUDE reports naming product code KWL, 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
20072—3611
20081—013
20090—221
20100—055
20112—051
20121—062
20130—089
20140—0107
20151—1223
20160—0210
20170—2347
20182—0294
20191—0415
20201—0270
20210—0107
20221—099
20230—048
20241—0143
2025332029
20262—1—
Cite this page

510(k) Report. “K872776: Profile Femoral Hip Prosthesis W/Porocoat.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K872776

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026