SpydrBlade Flex Instrument (PRD-RG1-001)— 510(k) K242774

Substantially Equivalent

Creo Medical, Ltd.

FDA 510(k) clearance K242774 for SpydrBlade Flex Instrument (PRD-RG1-001), Substantially Equivalent on 2025-06-06. Applicant: Creo Medical, Ltd..

Clearance details

Applicant: Creo Medical, Ltd.
Product code: Code KNS
Advisory panel: Gastroenterology, Urology
Date received: 2024-09-13
Decision date: 2025-06-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chepstow, GB

Download summary PDF View on FDA.gov ↗

Adverse events under product code KNS

product code KNS

Death: 44
Injury: 2,361
Malfunction: 4,771
Total: 7,176

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.