K251145
- 510(k) number
- K251145
- Device name
- Arthrex PushLock Suture Anchors
- Applicant
- Arthrex, Inc. FL · US
- Product code
- MBI — Fastener, Fixation, Nondegradable, Soft Tissue
- Decision date
- 2025-07-10
- Date received
- 2025-04-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K251145.pdf
Official FDA record: K251145
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.