Last synced on 14 November 2025 at 11:06 pm

SYNTHES(U.S.A.) ANTERIOR SPINAL PLATE

Page Type
Cleared 510(K)
510(k) Number
K925351
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
11/5/1993
Days to Decision
379 days
Submission Type
Summary

SYNTHES(U.S.A.) ANTERIOR SPINAL PLATE

Page Type
Cleared 510(K)
510(k) Number
K925351
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
11/5/1993
Days to Decision
379 days
Submission Type
Summary