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SYNTHES (U.S.A.) ANTERIOR CERVICAL VERTEBRAE PLATE

Page Type
Cleared 510(K)
510(k) Number
K926453
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
10/12/1993
Days to Decision
292 days
Submission Type
Summary

SYNTHES (U.S.A.) ANTERIOR CERVICAL VERTEBRAE PLATE

Page Type
Cleared 510(K)
510(k) Number
K926453
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
10/12/1993
Days to Decision
292 days
Submission Type
Summary