Last synced on 14 November 2025 at 11:06 pm

SYNTHES CERVIFIX SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K011969
510(k) Type
Special
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2001
Days to Decision
24 days
Submission Type
Summary

SYNTHES CERVIFIX SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K011969
510(k) Type
Special
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2001
Days to Decision
24 days
Submission Type
Summary