K240268
- 510(k) number
- K240268
- Device name
- Accu-Joint Hemi Implant
- Applicant
- Accufix Surgical, Inc. CT · US
- Product code
- KWD — Prosthesis, Toe, Hemi-, Phalangeal
- Decision date
- 2024-02-29
- Date received
- 2024-01-31
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K240268.pdf
Official FDA record: K240268
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.