Cleared Traditional

K855183 - COFIELD SHOULDER SYSTEM

K855183 is an FDA 510(k) clearance for COFIELD SHOULDER SYSTEM, manufactured by Richards Medical Co., 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.

K855183 · Richards Medical Co., Inc. · Orthopedic device
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Mar 1986
Decision
90d
Days
Class 2
Risk

K855183 is an FDA 510(k) clearance for the COFIELD SHOULDER SYSTEM. Classified as Prosthesis, Shoulder, Semi-constrained, Metal/polymer Cemented (product code KWS), Class II - Special Controls.

Submitted by Richards Medical Co., Inc. (Memphis, US). The FDA issued a Cleared decision on March 26, 1986 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 Richards Medical Co., Inc. devices

FDA 510(k) Submission Details - K855183

510(k) Number K855183 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 26, 1985
Decision Date March 26, 1986
Days to Decision 90 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
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 K855183.
INTERMEDICS SELECT SHOULDER ALL PLASTIC GLEN. COMP
K881836 · Intermedics Orthopedics · Aug 1988
FENLIN II SHOULDER PROSTHESIS
K870262 · Zimmer, Inc. · Apr 1987
OSTEONICS SHOULDER PROSTHESIS
K862535 · Osteonics Corp. · Sep 1986
COFIELD SHOULDER SYSTEM
K843624 · Richards Medical Co., Inc. · Jan 1985
MONOSPHERICAL GLENOID PROSTH. KEEL
K833410 · Howmedica Corp. · Nov 1983
UCLA SHOULDER
K801970 · Howmedica Corp. · Dec 1980