K250483
- 510(k) number
- K250483
- Device name
- PhotonBlade 3; PhotonBlade 3 Smoke Evacuation
- Applicant
- Stryker Instruments MI · US
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2025-09-09
- Date received
- 2025-02-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K250483.pdf
Official FDA record: K250483
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.