C-QUR V -PATCH MESH
FDA 510(k) clearance K090909 · decided 2009-06-04
Clearance details
- K-number
- K090909
- Device name
- C-QUR V -PATCH MESH
- Applicant
- Atrium Medical Corp.
- Decision
- Substantially Equivalent
- Date received
- 2009-04-01
- Decision date
- 2009-06-04
- Days to decision
- 64 days
- Clearance type
- Special
- Product code
- FTL
- Device class
- 2
- Regulation number
- 878.3300
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Hudson, NH, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| C-QUR V-Patch Mesh (All sizes and shapes). Intended for use in soft tissue deficiencies. recall (Z-1938-2013) | Atrium Medical Corporation | 2013-08-09 |
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| iCast Covered Stent System (P120003/S009) | Atrium Medical Corp. | 2025-12-22 |
| iCast Covered Stent System (P120003/S011) | Atrium Medical Corp. | 2025-09-12 |
| iCast Covered Stent System (P120003/S010) | Atrium Medical Corp. | 2025-08-20 |
| iCast Covered Stent System (P120003/S006) | Atrium Medical Corp. | 2025-07-07 |
| iCast Covered Stent System (P120003/S008) | Atrium Medical Corp. | 2025-05-01 |
| iCast Covered Stent System (P120003/S005) | Atrium Medical Corp. | 2024-08-07 |
| iCast Covered Stent System (P120003/S004) | Atrium Medical Corp. | 2024-07-24 |
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