FDA PMA FDA Class 3 Approved 🇺🇸 United States

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

PMA: P030042 · Supplement: S003 · Decision Jun 21, 2010
Classifications
1
FEI Numbers
8
Registration Numbers
8

Basic Information

Device Name
Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing
Trade Name
CONSERVE PLUS HIP RESURFACING SYSTEM NEW ENROLLMENT STUDY (NES) PROTOCOL
PMA Number
P030042
Supplement Number
S003
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 21, 2010
Date Received
January 21, 2010
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Postapproval Study Protocol - OSB
Expedited Review
N

Advisory Committee Statement

APPROVAL OF THE POST-APPROVAL STUDY PROTOCOL.

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