FDA PMA FDA Class 3 Approved 🇺🇸 United States

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

PMA: P040033 · Supplement: S024 · Decision Dec 11, 2015
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
S024
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
December 11, 2015
Date Received
November 21, 2013
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Labeling Change - PAS
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR AN UPDATE TO THE DEVICE LABELING TO INCLUDE THE RESULTS OF THE COMPLETED UNITED KINGDOM (UK) POST-APPROVAL STUDY.

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