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

Prosthesis, Intervertebral Disc

PMA: P060023 · Supplement: S004 · Decision Jan 11, 2013
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
S004
Device Class
FDA Class 3
Product Code
MJO
Generic Name
Prosthesis, intervertebral disc
Medical Specialty
Unknown
Advisory Committee
Orthopedic
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
January 11, 2013
Date Received
December 13, 2012
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

USE OF A NEW LOCATION FOR THE POROUS COATING PROCESS PERFORMED AT THE FIRM¿S SUPPLIER.

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