K233661 is an FDA 510(k) clearance for the Transorb? Self-Gripping Resorbable Mesh, a Mesh, Surgical, Absorbable, Abdominal Hernia (Class II — Special Controls, product code OWT), submitted by Sofradim Production (Tr?voux, FR). The FDA issued a Cleared decision on February 13, 2024, 90 days after receiving the submission on November 15, 2023. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.3300.
| 510(k) Number | K233661 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 15, 2023 |
| Decision Date | February 13, 2024 |
| Days to Decision | 90 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | OWT — Mesh, Surgical, Absorbable, Abdominal Hernia |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 878.3300 |
| Definition | For Reinforcement Of Soft Tissue Where Weakness Exists During Hernia Repair. |