FDA Product Code
FDA Product Code KYK — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Orthopedic
- 21 CFR Citation
- 888.3500
510(k) Clearances — 3 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K880826 | MICROLOC(TM) POROUS COATED UNICONDYLAR KNEE SYSTEM | Johnson & Johnson Professionals, Inc. | 1988-03-14 | Traditional | PDF ↗ |
| K871118 | MODIFIED TOWNLEY UNICONDYLAR KNEE | Depuy, Inc. | 1987-04-06 | Traditional | PDF ↗ |
| K851341 | SYNATOMIC VARIABLE FIT TIBIAL PLATEAU | Depuy, Inc. | 1985-07-15 | Traditional | PDF ↗ |
Product code KYK · Class II · Orthopedic. Data: openFDA.