Last synced on 25 April 2025 at 11:05 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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