FDA PMA FDA Class 3 Approved 🇺🇸 United States

Prosthesis, Intervertebral Disc

PMA: P060023 · Supplement: S002 · Decision Sep 13, 2012
Classifications
1
FEI Numbers
73
Registration Numbers
73

Basic Information

Device Name
Prosthesis, Intervertebral Disc
Trade Name
BRYAN CERVICAL DISC
PMA Number
P060023
Supplement Number
S002
Device Class
FDA Class 3
Product Code
MJO
Generic Name
Prosthesis, intervertebral disc
Medical Specialty
Unknown
Advisory Committee
Orthopedic
Decision
Approved
Decision Code
APPR
Decision Date
September 13, 2012
Date Received
April 15, 2011
Supplement Type
135 Review Track For 30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR A CHANGE TO THE INJECTION MOLDING PROCESS.

Classifications

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

Product Code Device Name
MJO Prosthesis, Intervertebral Disc