FDA PMA FDA Class 3 Approved 🇺🇸 United States

Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing

PMA: P040033 · Supplement: S005 · Decision Jun 27, 2007
Classifications
1
FEI Numbers
8
Registration Numbers
8

Basic Information

Device Name
Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing
Trade Name
BIRMINGHAM HIP RESURFACING (BHR) SYSTEM
PMA Number
P040033
Supplement Number
S005
Device Class
FDA Class 3
Product Code
NXT
Generic Name
Prosthesis, hip, semi-constrained, metal/metal, resurfacing
Medical Specialty
Unknown
Advisory Committee
Orthopedic
Decision
Approved
Decision Code
APPR
Decision Date
June 27, 2007
Date Received
April 2, 2007
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR THE ADDITION AND MODIFICATION OF SURGICAL INSTRUMENTS FOR USE WITH THE BHR SYSTEM AND REVISIONS TO THE SURGICAL TECHNIQUE.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NXT Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing