FDA PMA FDA Class 3 Approved 🇺🇸 United States

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

PMA: P070026 · Supplement: S113 · Decision Oct 23, 2024
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
CERAMAX Ceramic Total Hip System
PMA Number
P070026
Supplement Number
S113
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
Approved
Decision Code
APPR
Decision Date
October 23, 2024
Date Received
July 25, 2024
Supplement Type
Real-Time Process
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

approval for MRI Compatibility labeling updates and other minor labeling updates

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