K251844 is an FDA 510(k) clearance for the Kerecis SurgiBind (50241). This device is classified as a Mesh, Surgical, Collagen, Plastic And Reconstructive Surgery (Class II - Special Controls, product code OXH).
Submitted by Kerecis Limited (Isafjordur, IS). The FDA issued a Cleared decision on July 15, 2025, 29 days after receiving the submission on June 16, 2025.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.3300. For Reinforcement Of Soft Tissue Where Weakness Exists In Plastic And Reconstructive Surgery..
| 510(k) Number | K251844 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 16, 2025 |
| Decision Date | July 15, 2025 |
| Days to Decision | 29 days |
| Submission Type | Special |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | OXH - Mesh, Surgical, Collagen, Plastic And Reconstructive Surgery |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.3300 |
| Definition | For Reinforcement Of Soft Tissue Where Weakness Exists In Plastic And Reconstructive Surgery. |