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SYNTHES CRANIOFACIAL PLATE AND SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K080331
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/2008
Days to Decision
84 days
Submission Type
Summary

SYNTHES CRANIOFACIAL PLATE AND SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K080331
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/2008
Days to Decision
84 days
Submission Type
Summary