FDA PMA FDA Class 3 Approved 🇺🇸 United States

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

PMA: P040033 · Supplement: S038 · Decision Jan 19, 2024
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
S038
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
January 19, 2024
Date Received
December 20, 2023
Supplement Type
Special (Immediate Track)
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

a change to the Catalog Item (CI) reference codes (i.e., US market only) for the BIRMINGHAM HIP RESURFACING SYSTEM femoral head and acetabular cup implants

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