NDM
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Pin, Fixation, Threaded, Metallic
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3040
- Medical specialty
- Orthopedic
- Flags
- Implant
- Adverse events (MAUDE)
- 2020: 89
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| REPROCESSED PINS (K100707) | Sterilmed, Inc. | 2010-06-25 |
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Every clearance here is in the API, with alerts when new ones post.