Cleared Traditional

K926120 - CONTOUR FEMORAL HIP STEM WITH POROCOAT

K926120 is the FDA 510(k) clearance for CONTOUR FEMORAL HIP STEM WITH POROCOAT by Depuy, Inc.. It is a Class 2 Orthopedic device (product code KWL) cleared through the Traditional 510(k) pathway after a 118-day FDA review.

K926120 · Depuy, Inc. · Orthopedic device
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Optimized for regulatory review, auditing and printing
Mar 1993
Decision
118d
Days
Class 2
Risk

K926120 is an FDA 510(k) clearance for the CONTOUR FEMORAL HIP STEM WITH POROCOAT. Classified as Prosthesis, Hip, Hemi-, Femoral, Metal (product code KWL), Class II - Special Controls.

Submitted by Depuy, Inc. (Warsaw, US). The FDA issued a Cleared decision on March 31, 1993 after a review of 118 days - within the typical 510(k) review window.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3360 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Orthopedic review framework, consistent with the majority of Class II 510(k) submissions.

View all Depuy, Inc. devices

Submission Details

510(k) Number K926120 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 03, 1992
Decision Date March 31, 1993
Days to Decision 118 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
4d faster than avg
Panel avg: 122d · This submission: 118d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KWL Prosthesis, Hip, Hemi-, Femoral, Metal
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3360
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 - KWL Prosthesis, Hip, Hemi-, Femoral, Metal

All 77
Devices cleared under the same product code (KWL) and FDA review panel - the closest regulatory comparables to K926120.
ULTIMA AUGMENTED UHMWPE CUP
K950563 · Johnson & Johnson Professionals, Inc. · Jun 1995
ZIRCONIUM ALLOY UNI-POLAR HEAD
K934353 · Smith & Nephew Richards, Inc. · Apr 1994
TITANIUM NITRIDE COATED HEMI-HEAD COMPONENT
K924050 · Orthomet, Inc. · Aug 1993
OSTRONCS HEMI-HIP STEM SERIES
K922146 · Osteonics Corp. · Aug 1992
OMNIFLEX M-HA HIP STEM SERIES
K920193 · Stryker Corp. · Jun 1992
OMNIFIT M-HA HIP STEM SERIES
K920231 · Stryker Corp. · Jun 1992