K233893
- 510(k) number
- K233893
- Device name
- AlphaVent Knotless SP PEEK Anchor
- Applicant
- Stryker Endoscopy CA · US
- Product code
- MBI — Fastener, Fixation, Nondegradable, Soft Tissue
- Decision date
- 2024-01-25
- Date received
- 2023-12-08
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K233893.pdf
Official FDA record: K233893
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.