K233991 is an FDA 510(k) clearance for the CanGaroo RM Antibacterial Envelope. This device is classified as a Mesh, Surgical (Class II - Special Controls, product code FTM).
Submitted by Elutia, Inc. (Roswell, US). The FDA issued a Cleared decision on June 14, 2024, 179 days after receiving the submission on December 18, 2023.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.3300.
| 510(k) Number | K233991 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 18, 2023 |
| Decision Date | June 14, 2024 |
| Days to Decision | 179 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 |