Class Class II

SpydrBlade Flex Instrument (PRD-RG1-001) (K242774)

K242774 2025-06-06 Traditional
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Description

SpydrBlade Flex Instrument (PRD-RG1-001) by Creo Medical, Ltd., an FDA 510(k) cleared gastroenterology, urology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK242774
Clearance Date2025-06-06
Clearance TypeTraditional
Product CodeKNS
Regulation Number876.4300

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