K260294
- 510(k) number
- K260294
- Device name
- SF Push-in Anchor
- Applicant
- Surgical Fusion Technologies GmbH CH
- Product code
- MAI — Fastener, Fixation, Biodegradable, Soft Tissue
- Decision date
- 2026-03-27
- Date received
- 2026-01-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.2 MB · U.S. public domain
Also available from FDA: K260294.pdf
Official FDA record: K260294
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.