K242494
- 510(k) number
- K242494
- Device name
- OsseoFit Interfacing Anchor; OsseoFit Bone Tunnel Construct
- Applicant
- Riverpoint Medical, LLC OR · US
- Product code
- MBI — Fastener, Fixation, Nondegradable, Soft Tissue
- Decision date
- 2024-11-26
- Date received
- 2024-08-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.4 MB · U.S. public domain
Also available from FDA: K242494.pdf
Official FDA record: K242494
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.