K151437 is an FDA 510(k) clearance for the ProLite Mesh, ProLite Ultra Mesh, ProLoop Mesh Plug. This device is classified as a Mesh, Surgical, Polymeric (Class II - Special Controls, product code FTL).
Submitted by Atrium Medical Corporation (Hudson, US). The FDA issued a Cleared decision on August 27, 2015, 90 days after receiving the submission on May 29, 2015.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.3300.
| 510(k) Number | K151437 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 29, 2015 |
| Decision Date | August 27, 2015 |
| Days to Decision | 90 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | FTL - Mesh, Surgical, Polymeric |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.3300 |