Last synced on 14 November 2025 at 11:06 pm

SYNTHES CERVIFIX SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K990965
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/1999
Days to Decision
101 days
Submission Type
Summary

SYNTHES CERVIFIX SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K990965
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/1999
Days to Decision
101 days
Submission Type
Summary