K162752 is an FDA 510(k) clearance for the ARTIA Reconstructive Tissue Matrix Perforated. This device is classified as a Mesh, Surgical (Class II - Special Controls, product code FTM).
Submitted by Lifecell Corporation (Branchburg, US). The FDA issued a Cleared decision on February 24, 2017, 147 days after receiving the submission on September 30, 2016.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.3300.
| 510(k) Number | K162752 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 30, 2016 |
| Decision Date | February 24, 2017 |
| Days to Decision | 147 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | FTM — Mesh, Surgical |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.3300 |