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SYNTHES CERVIFIX SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K001864
510(k) Type
Special
Applicant
SYNTHES SPINE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2000
Days to Decision
30 days
Submission Type
Summary

SYNTHES CERVIFIX SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K001864
510(k) Type
Special
Applicant
SYNTHES SPINE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2000
Days to Decision
30 days
Submission Type
Summary