K233971
- 510(k) number
- K233971
- Device name
- Arthrex AlloSync PushLock Suture Anchor
- Applicant
- Arthrex, Inc. FL · US
- Product code
- MAI — Fastener, Fixation, Biodegradable, Soft Tissue
- Decision date
- 2024-06-04
- Date received
- 2023-12-15
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K233971.pdf
Official FDA record: K233971
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.