FDA Product Code
FDA Product Code KWK — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Orthopedic
- 21 CFR Citation
- 888.3030
510(k) Clearances — 1 record
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K931682 | CANNULATED MALLEOLAR SCREW | Onyx Medical Corp. | 1994-04-05 | Traditional | PDF ↗ |
Product code KWK · Class II · Orthopedic. Data: openFDA.