Last synced on 25 January 2026 at 3:41 am

SpydrBlade Flex Instrument (PRD-RG1-001)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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