NEH
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Anchor, Fascial
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.4300
- Medical specialty
- General, Plastic Surgery
- Flags
- Implant
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| Record | Firm | Date | Builder |
|---|---|---|---|
| AMS FASCIAL-ANCHORING SYSTEM (K010277) | American Medical Systems, Inc. | 2001-03-26 | + Add |
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Every clearance here is in the API, with alerts when new ones post.