Cleared Traditional

K843190 - HAP ACETABULAR CUP

K843190 is an FDA 510(k) clearance for HAP ACETABULAR CUP, manufactured by Depuy, Inc.. The device is a Class 2 Orthopedic device with product code JDI cleared through the Traditional 510(k) pathway after a 95-day FDA review.

K843190 · Depuy, Inc. · Orthopedic device
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Nov 1984
Decision
95d
Days
Class 2
Risk

K843190 is an FDA 510(k) clearance for the HAP ACETABULAR CUP. Classified as Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented (product code JDI), Class II - Special Controls.

Submitted by Depuy, Inc. (Warsaw, US). The FDA issued a Cleared decision on November 16, 1984 after a review of 95 days - within the typical 510(k) review window.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3350 - 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

FDA 510(k) Submission Details - K843190

510(k) Number K843190 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 13, 1984
Decision Date November 16, 1984
Days to Decision 95 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
27d faster than avg
Panel avg: 122d · This submission: 95d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JDI Device Classification - Class 2, Special Controls

Product Code JDI Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3350
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 - JDI Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented

All 516
Devices cleared under the same product code (JDI) and FDA review panel - the closest regulatory comparables to K843190.
CFE ACETABULAR CUP
K844941 · Biomet, Inc. · Mar 1985
BROOKER ACETABULAR CUP
K845005 · Biomet, Inc. · Feb 1985
LORD SCREW RING ACETABULAR COMPONENT
K844028 · Howmedica Corp. · Feb 1985
TITANIUM HIP 1019
K843909 · Depuy, Inc. · Nov 1984
DORR HIP PROSTHESIS FEMORAL COMPONENT
K842360 · Carbomedics, Inc. · Oct 1984
BIAS TOTAL HIP
K842906 · Zimmer, Inc. · Aug 1984