Cleared Traditional

K915655 - STABILITY FEMORAL PROSTHESIS W/HAP

K915655 is the FDA 510(k) clearance for STABILITY FEMORAL PROSTHESIS W/HAP by Depuy, Inc.. It is a Class 2 Orthopedic device (product code MEH) cleared through the Traditional 510(k) pathway after a 789-day FDA review.

K915655 · Depuy, Inc. · Orthopedic device
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Optimized for regulatory review, auditing and printing
Feb 1994
Decision
789d
Days
Class 2
Risk

K915655 is an FDA 510(k) clearance for the STABILITY FEMORAL PROSTHESIS W/HAP. Classified as Prosthesis, Hip, Semi-constrained, Uncemented, Metal / Polymer, Non-porous, Calcium Phosphate (product code MEH), Class II - Special Controls.

Submitted by Depuy, Inc. (Warsaw, US). The FDA issued a Cleared decision on February 14, 1994 after a review of 789 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3353 - the FDA orthopedic device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Orthopedic submissions.

View all Depuy, Inc. devices

Submission Details

510(k) Number K915655 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 18, 1991
Decision Date February 14, 1994
Days to Decision 789 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
667d slower than avg
Panel avg: 122d · This submission: 789d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code MEH Prosthesis, Hip, Semi-constrained, Uncemented, Metal / Polymer, Non-porous, Calcium Phosphate
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3353
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Orthopedic devices follow this clearance model.

Regulatory Peers - MEH Prosthesis, Hip, Semi-constrained, Uncemented, Metal / Polymer, Non-porous, Calcium Phosphate

All 132
Devices cleared under the same product code (MEH) and FDA review panel - the closest regulatory comparables to K915655.
TECHMEDICA CONTINUUM HIP WITH HA COATING
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K935990 · Implex Corp. · Jul 1994
HA TI-FIT ACETABULAR AND FEMORAL COMPONENT
K922621 · Smith & Nephew Richards, Inc. · Mar 1994
HA ANATOMIC HIP PROSTH W/TI-NIDIUM SURF HARD PROCE
K925607 · Zimmer, Inc. · Nov 1993
CONTOUR FEMORAL HIP STEM W/HYDROAPATITE COATING
K926299 · Depuy, Inc. · Oct 1993
H-220 PRESS-FIT ACETABULAR CUP SYSTEM
K926134 · Implex Corp. · Oct 1993