Cleared Traditional

K974044 - GLOBAL TOTAL SHOULDER ECCENTRIC HUMERAL...

K974044 is an FDA 510(k) clearance for GLOBAL TOTAL SHOULDER ECCENTRIC HUMERAL..., manufactured by DePuy Orthopaedics, Inc.. The device is a Class 2 Orthopedic device with product code KWS cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K974044 · DePuy Orthopaedics, Inc. · Orthopedic device
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Optimized for regulatory review, auditing and printing
Jan 1998
Decision
90d
Days
Class 2
Risk

K974044 is an FDA 510(k) clearance for the GLOBAL TOTAL SHOULDER ECCENTRIC HUMERAL HEAD. Classified as Prosthesis, Shoulder, Semi-constrained, Metal/polymer Cemented (product code KWS), Class II - Special Controls.

Submitted by DePuy Orthopaedics, Inc. (Warsaw, US). The FDA issued a Cleared decision on January 22, 1998 after a review of 90 days - within the typical 510(k) review window.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3660 - 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 Orthopaedics, Inc. devices

FDA 510(k) Submission Details - K974044

510(k) Number K974044 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 24, 1997
Decision Date January 22, 1998
Days to Decision 90 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
32d faster than avg
Panel avg: 122d · This submission: 90d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KWS Device Classification - Class 2, Special Controls

Product Code KWS Prosthesis, Shoulder, Semi-constrained, Metal/polymer Cemented
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3660
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 - KWS Prosthesis, Shoulder, Semi-constrained, Metal/polymer Cemented

All 156
Devices cleared under the same product code (KWS) and FDA review panel - the closest regulatory comparables to K974044.
ANATOMICA GLENOID COMPONENT
K990136 · Sulzer Orthopedics, Inc. · Mar 1999
ANATOMICA HUMERAL STEM/HEAD COMPONENTS
K990137 · Sulzer Orthopedics, Inc. · Feb 1999
DEPUY GLOBAL SHOULDER GLENOID
K981487 · DePuy Orthopaedics, Inc. · Jul 1998
SELECT SHOULDER OFFSET HUMERAL HEAD COMPONENTS
K971715 · Sulzer Orthopedics, Inc. · Aug 1997
SELECT SHOULDER CONCENTRIC HUMERAL HEAD COMPONENTS
K962224 · Intermedics Orthopedics · Aug 1996
OSTEONICS ALL POLYETHYLENE GLENOID SHOULDER COMPONENT
K962082 · Osteonics Corp. · Aug 1996