K251844
- 510(k) number
- K251844
- Device name
- Kerecis SurgiBind (50241)
- Applicant
- Kerecis Limited IS
- Product code
- OXH — Mesh, Surgical, Collagen, Plastic And Reconstructive
- Decision date
- 2025-07-15
- Date received
- 2025-06-16
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K251844.pdf
Official FDA record: K251844
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.