Cleared Traditional

K873514 - JOHNSON & JOHNSON BIPOLAR ENDOPROTHESIS

K873514 is the FDA 510(k) clearance for JOHNSON & JOHNSON BIPOLAR ENDOPROTHESIS by Johnson & Johnson Professionals, Inc.. It is a Class 2 Orthopedic device (product code KWY) cleared through the Traditional 510(k) pathway after a 24-day FDA review.

K873514 · Johnson & Johnson Professionals, Inc. · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 1987
Decision
24d
Days
Class 2
Risk

K873514 is an FDA 510(k) clearance for the JOHNSON & JOHNSON BIPOLAR ENDOPROTHESIS. Classified as Prosthesis, Hip, Hemi-, Femoral, Metal/polymer, Cemented Or Uncemented (product code KWY), Class II - Special Controls.

Submitted by Johnson & Johnson Professionals, Inc. (Raynham, US). The FDA issued a Cleared decision on September 24, 1987 after a review of 24 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3390 - 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 Johnson & Johnson Professionals, Inc. devices

Submission Details

510(k) Number K873514 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 31, 1987
Decision Date September 24, 1987
Days to Decision 24 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
98d faster than avg
Panel avg: 122d · This submission: 24d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KWY Prosthesis, Hip, Hemi-, Femoral, Metal/polymer, Cemented Or Uncemented
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3390
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 - KWY Prosthesis, Hip, Hemi-, Femoral, Metal/polymer, Cemented Or Uncemented

All 76
Devices cleared under the same product code (KWY) and FDA review panel - the closest regulatory comparables to K873514.
ZIMMER BEADED THREADED ACETABULAR CUP
K884658 · Zimmer, Inc. · Nov 1988
CORIN BIPOLAR PROSTHESIS
K881289 · Orthopedic Systems, Inc. · Jun 1988
IOI BIPOLAR PROSTHESIS
K873815 · Intermedics Orthopedics · Oct 1987
BI-ARTICULAR II HIP DEVICE
K872019 · Zimmer, Inc. · Jul 1987
KIRSCHNER UNIVERSAL BIPOLAR ENDOPROSTHETIC HEAD
K862057 · Kirschner Medical Corp. · Jul 1986
SLR BIPOLAR HIP ENDOPROSTHESIS
K861566 · Dow Corning Wright · May 1986