HXO
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Pusher, Socket
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 888.4540
- Medical specialty
- Orthopedic
- Adverse events (MAUDE)
- 1996: 2 · 1997: 3 · 1999: 1 · 2007: 2 · 2010: 7 · 2013: 6
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 |
|---|---|---|
| ACETABULAR CUP PUSHER/IMPACTOR (K885305) | Cobot Medical Corp. | 1989-02-08 |
| ACETABULAR CEMENT COMPRESSOR (K803165) | Zimmer, Inc. | 1980-12-31 |
| INSERTEO, META.-PHAL.&THUMB CARPO-META (K771072) | Depuy, Inc. | 1977-06-27 |
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Every clearance here is in the API, with alerts when new ones post.