FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented

PMA: P070026 · Supplement: S005 · Decision Apr 26, 2012
Classifications
1
FEI Numbers
34
Registration Numbers
34

Basic Information

Device Name
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented
Trade Name
DEPUY CERAMAX CERAMIC TOTAL HIP SYSTEM
PMA Number
P070026
Supplement Number
S005
Device Class
FDA Class 3
Product Code
MRA
Generic Name
Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented
Medical Specialty
Unknown
Advisory Committee
Orthopedic
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
April 26, 2012
Date Received
March 27, 2012
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

CHANGES TO THE STERILE BARRIER PACKAGE SEALING PROCESS USED FOR THE CERAMIC FEMORAL HEADS AND ACETABULAR LINERS.

Classifications

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

Product Code Device Name
MRA Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented