Last synced on 18 April 2025 at 11:05 pm

SYNTHES REPROCESSED EXTERNAL FIXATION DEVICES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033158
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2003
Days to Decision
36 days
Submission Type
Summary

SYNTHES REPROCESSED EXTERNAL FIXATION DEVICES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033158
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2003
Days to Decision
36 days
Submission Type
Summary