K242774
- 510(k) number
- K242774
- Device name
- SpydrBlade Flex Instrument (PRD-RG1-001)
- Applicant
- Creo Medical, Ltd. GB
- Product code
- KNS — Unit, Electrosurgical, Endoscopic (With Or Without A
- Decision date
- 2025-06-06
- Date received
- 2024-09-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K242774.pdf
Official FDA record: K242774
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.