HXR
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Spatula, Orthopedic
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.4800
- Medical specialty
- General, Plastic Surgery
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| MICRO ENDOSCOPE-STAINLESS STEEL, MODEL MMD-1300, MICRO ENDOSCOPE-POLYIMIDE,MODEL MMD-1400 (K983882) | Micro-Medical Devices, Inc. | 1999-03-15 |
| VIDEO ARTHROSCOPE, 1.7MM X 55 MM (K873387) | Arthropedics, Inc. | 1987-11-25 |
| RAYLOR FUSION FUNNEL (K872281) | Cedar Surgical, Inc. | 1987-11-02 |
| H-H HUNTER PASSIVE TENDON IMPLANT (K853436) | Holter-Hausner Intl. | 1985-10-16 |
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Every clearance here is in the API, with alerts when new ones post.