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

Joint, Temporomandibular, Implant

PMA: P000023 · Supplement: S011 · Decision Feb 13, 2015
Classifications
1
FEI Numbers
5
Registration Numbers
5

Basic Information

Device Name
Joint, Temporomandibular, Implant
Trade Name
TMJ FOSSA-EMINENCE AND CONDYLAR PROSTHESIS SYSTEM
PMA Number
P000023
Supplement Number
S011
Device Class
FDA Class 3
Product Code
LZD
Generic Name
Joint, temporomandibular, implant
Regulation Number
872.3940
Medical Specialty
Dental
Advisory Committee
Dental
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
February 13, 2015
Date Received
January 16, 2015
Supplement Type
30-Day Notice
Expedited Review
N

Advisory Committee Statement

CHANGES IN TWO CLEANING PROCESSES.

Classifications

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

Product Code Device Name
LZD Joint, Temporomandibular, Implant