Cleared Traditional

K871656 - ORTHOMET AUSTIN-MOORE SYSTEM

K871656 is an FDA 510(k) clearance for ORTHOMET AUSTIN-MOORE SYSTEM, manufactured by Orthomet, Inc.. The device is a Class 2 Orthopedic device with product code KWL cleared through the Traditional 510(k) pathway after a 42-day FDA review.

K871656 · Orthomet, Inc. · Orthopedic device
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Jun 1987
Decision
42d
Days
Class 2
Risk

K871656 is an FDA 510(k) clearance for the ORTHOMET AUSTIN-MOORE SYSTEM. Classified as Prosthesis, Hip, Hemi-, Femoral, Metal (product code KWL), Class II - Special Controls.

Submitted by Orthomet, Inc. (Minneapolis, US). The FDA issued a Cleared decision on June 9, 1987 after a review of 42 days - a notably fast clearance cycle.

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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Orthomet, Inc. devices

FDA 510(k) Submission Details - K871656

510(k) Number K871656 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 28, 1987
Decision Date June 09, 1987
Days to Decision 42 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
80d faster than avg
Panel avg: 122d · This submission: 42d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KWL Device Classification - Class 2, Special Controls

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 81
Devices cleared under the same product code (KWL) and FDA review panel - the closest regulatory comparables to K871656.
PROFILE FEMORAL HIP PROSTHESIS W/POROCOAT
K872776 · Depuy, Inc. · Aug 1987
POROCOAT (R) PROXIMAL FEMORAL THIRD PROSTHESIS
K872025 · Depuy, Inc. · Aug 1987
TRI-LOCK MODIFIED FEMORAL PROSTHESIS
K872878 · Depuy, Inc. · Aug 1987
BROOKER BIO-GROOVE FEMORAL COMPONENT
K864085 · Biomet, Inc. · Jan 1987
BIO-FIT HIP SYSTEM
K854791 · Richards Medical Co., Inc. · Feb 1986
MUELLER CURVED STEM HEMI-PROSTHESIS
K853662 · Protek, Inc. · Sep 1985