Last synced on 14 November 2025 at 11:06 pm

CLAMPFIX

Page Type
Cleared 510(K)
510(k) Number
K090605
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/2009
Days to Decision
245 days
Submission Type
Summary

CLAMPFIX

Page Type
Cleared 510(K)
510(k) Number
K090605
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/2009
Days to Decision
245 days
Submission Type
Summary