K262369
- 510(k) number
- K262369
- Device name
- AIR+ All-Inside Meniscal Repair Device, Curved Up;AIR+ All-Inside Meniscal Repair Device, Curved Down
- Applicant
- Stryker Endoscopy CA · US
- Product code
- MBI — Fastener, Fixation, Nondegradable, Soft Tissue
- Decision date
- 2026-07-30
- Date received
- 2026-07-10
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K262369.pdf
Official FDA record: K262369
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.