The following data is part of a premarket notification filed by Biomet, Inc. with the FDA for Agc Total Knee Prosthesis.
Device ID | K833921 |
510k Number | K833921 |
Device Name: | AGC TOTAL KNEE PROSTHESIS |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | BIOMET, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | JWH |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1983-11-14 |
Decision Date | 1984-01-31 |