FDA Product Code
FDA Product Code NDL — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Orthopedic
- 21 CFR Citation
- 888.3040
510(k) Clearances — 2 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K010847 | K'FIX | Avanta Orthopaedics, Inc. | 2001-06-19 | Traditional | PDF ↗ |
| K010545 | TBW | Tri-Med, Inc. | 2001-06-06 | Traditional | PDF ↗ |
Product code NDL · Class II · Orthopedic. Data: openFDA.