NCA
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Clip, Implantable, For Coronary Artery Bypass Graft (Cabg)
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.4300
- Medical specialty
- General, Plastic Surgery
- Flags
- Implant
- Adverse events (MAUDE)
- 2007: 3
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 |
|---|---|---|
| COALESCENT SURGICAL U-CLIP (K013664) | Coalescent Surgical | 2002-01-24 |
| CORLINK AAD (3.5 TO 6.0 M M OUTER DIAMETER VESSELS),MODEL 200-064, CORLINK AAD (2.0 TO 4.0 MM OUTER DIAMETER VESSELS), M (K011589) | Bypass , Ltd. | 2001-12-26 |
| SYMMETRY AORTIC CLIP SYSTEM (K003446) | St. Jude Medical Cardiovascular Group, Inc. | 2001-05-21 |
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Every clearance here is in the API, with alerts when new ones post.