Last synced on 23 May 2025 at 11:06 pm

SYNTHES (USA) CRANIOFACIAL PLATES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040272
510(k) Type
Special
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/2004
Days to Decision
18 days
Submission Type
Summary

SYNTHES (USA) CRANIOFACIAL PLATES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040272
510(k) Type
Special
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/2004
Days to Decision
18 days
Submission Type
Summary