Product code KYK— Orthopedic
MICROLOC(TM) POROUS COATED UNICONDYLAR KNEE SYSTEM
- Classification name
- Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Composite
- Device class
- Class 2
- Regulation
- 21 CFR 888.3500
- Advisory panel
- Orthopedic
- Total cleared
- 3
- First cleared
- Most recent
Market context for product code KYK
FDA has cleared devices under product code KYK between 1985 and 1988, filed by 2 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
- 1988
- 1987
- 1985
Top applicants under product code KYK
Recent clearances under product code KYK
Data sourced from openFDA. This site is unofficial and independent of the FDA.