Cleared Traditional

K853916 - P.M. HIP-FEMORAL PROSTHESIS

K853916 is an FDA 510(k) clearance for P.M. HIP-FEMORAL PROSTHESIS, manufactured by Advanced Biosearch Assn.. 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.

K853916 · Advanced Biosearch Assn. · Orthopedic device
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Dec 1985
Decision
95d
Days
Class 2
Risk

K853916 is an FDA 510(k) clearance for the P.M. HIP-FEMORAL PROSTHESIS. Classified as Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented (product code JDI), Class II - Special Controls.

Submitted by Advanced Biosearch Assn. (Danville, US). The FDA issued a Cleared decision on December 27, 1985 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 Advanced Biosearch Assn. devices

FDA 510(k) Submission Details - K853916

510(k) Number K853916 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 23, 1985
Decision Date December 27, 1985
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 474
Devices cleared under the same product code (JDI) and FDA review panel - the closest regulatory comparables to K853916.
MODULAR PRESS FIT (MPF) STEM
K855200 · Depuy, Inc. · Apr 1986
CONICAL COLLAR HIP PROSTHESIS POROUS COATED
K860002 · Kirschner Medical Corp. · Apr 1986
HPS II SMOOTH STEM
K860701 · Depuy, Inc. · Mar 1986
ARTHOPOR-ACETABULAR COMPONENT
K844050 · Joint Medical Products Corp. · Dec 1985
P.C.A. UNIVERSAL ACETABULAR COMPONENT SYSTEM
K853886 · Howmedica Corp. · Nov 1985
MULLER SELF LOCKING TOTAL HIP
K853768 · Protek, Inc. · Nov 1985