Last synced on 23 May 2025 at 11:06 pm

SYNTHES (USA) MIDFACE DISTRACTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010499
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2001
Days to Decision
71 days
Submission Type
Summary

SYNTHES (USA) MIDFACE DISTRACTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010499
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2001
Days to Decision
71 days
Submission Type
Summary