KYK · Class II · 21 CFR 888.3500

FDA Product Code KYK: Prosthesis, Knee, Femorotibial, Semi-constrained, Cemented, Metal/composite

Leading manufacturers include Depuy, Inc. and Johnson & Johnson Professionals, Inc..

3
Total
3
Cleared
45d
Avg days
1985
Since

FDA 510(k) Cleared Prosthesis, Knee, Femorotibial, Semi-constrained, Cemented, Metal/composite Devices (Product Code KYK)

3 devices
1–3 of 3
Cleared Mar 14, 1988
MICROLOC(TM) POROUS COATED UNICONDYLAR KNEE SYSTEM
K880826
Johnson & Johnson Professionals, Inc.
Orthopedic · 13d
Cleared Apr 06, 1987
MODIFIED TOWNLEY UNICONDYLAR KNEE
K871118
Depuy, Inc.
Orthopedic · 18d
Cleared Jul 15, 1985
SYNATOMIC VARIABLE FIT TIBIAL PLATEAU
K851341
Depuy, Inc.
Orthopedic · 103d

About Product Code KYK - Regulatory Context