FDA PMA FDA Class 3 Approved 🇺🇸 United States

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

PMA: P040033 · Supplement: S011 · Decision Jun 9, 2009
Classifications
1
FEI Numbers
8
Registration Numbers
8

Basic Information

Device Name
Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing
Trade Name
BIRMINGHAM HIP RESURFACING SYSTEM
PMA Number
P040033
Supplement Number
S011
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 9, 2009
Date Received
April 17, 2009
Supplement Type
Real-Time Process
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR THE MODIFICATION OF THE BHR/R3 MODULAR RESURFACING SURGICAL TECHNIQUE ADDENDUM.

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