HTH
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Protractor
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 888.4600
- Medical specialty
- Orthopedic
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| SHORTENING OSTEOTOMY GUIDE (K861576) | Osteotomy Guide Co. | 1986-05-12 |
| REESE OSTEOTOMY GUIDE SYS (K841470) | Osteotomy Guide Co. | 1984-05-23 |
| ORTHO-LEVEL (K822305) | Frontier Products | 1982-08-20 |
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