Last synced on 14 November 2025 at 11:06 pm

SpydrBlade Flex Instrument (PRD-RG1-001)

Page Type
Cleared 510(K)
510(k) Number
K242774
510(k) Type
Traditional
Applicant
Creo Medical Ltd
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
6/6/2025
Days to Decision
266 days
Submission Type
Summary

SpydrBlade Flex Instrument (PRD-RG1-001)

Page Type
Cleared 510(K)
510(k) Number
K242774
510(k) Type
Traditional
Applicant
Creo Medical Ltd
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
6/6/2025
Days to Decision
266 days
Submission Type
Summary