K232683
- 510(k) number
- K232683
- Device name
- Knotilus+ PEEK Knotless Anchor
- Applicant
- Stryker Endoscopy CA · US
- Product code
- MBI — Fastener, Fixation, Nondegradable, Soft Tissue
- Decision date
- 2023-10-24
- Date received
- 2023-09-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K232683.pdf
Official FDA record: K232683
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.