K041140 is an FDA 510(k) clearance for the ACELL UBM SURGICAL MESH ML AND MLPLUS. This device is classified as a Mesh, Surgical (Class II - Special Controls, product code FTM).
Submitted by Acell, Inc. (Chevy Chase, US). The FDA issued a Cleared decision on July 7, 2004, 68 days after receiving the submission on April 30, 2004.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.3300.
| 510(k) Number | K041140 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 30, 2004 |
| Decision Date | July 07, 2004 |
| Days to Decision | 68 days |
| Submission Type | Abbreviated |
| 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 |