K241906
- 510(k) number
- K241906
- Device name
- BioBrace® Reinforced Implant
- Applicant
- Conmed Corporation NY · US
- Product code
- OWW — Mesh, Surgical, Absorbable, Orthopaedics, Reinforcem
- Decision date
- 2024-07-29
- Date received
- 2024-07-01
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K241906.pdf
Official FDA record: K241906
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.