FDA Product Code
FDA Product Code ORQ — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- General, Plastic Surgery
- 21 CFR Citation
- 878.3300
510(k) Clearances — 6 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K250395 | BioBrace ® RC Delivery System | Conmed Corporation | 2025-04-07 | Traditional | PDF ↗ |
| K130782 | ACCUMESH DEPLOYMENT SYSTEM | Covidien, LLC | 2013-04-05 | Special | PDF ↗ |
| K123066 | ACCUMESH DEPLOYMENT SYSTEM | Covidien, LLC | 2012-10-16 | Special | PDF ↗ |
| K121139 | ACCUMESH DEPLOYMENT SYSTEM | Covidien, LLC | 2012-05-02 | Special | PDF ↗ |
| K103269 | PATCHASSIST LARGE | Polytouch Medical, Ltd. | 2010-11-23 | Special | PDF ↗ |
| K101218 | PATCHASSIST | Polytouch Medical, Ltd. | 2010-06-17 | Traditional | PDF ↗ |
Product code ORQ · Class II · General, Plastic Surgery. Data: openFDA.