Last synced on 23 May 2025 at 11:06 pm

SYNTHES MIDFACE DISTRACTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022005
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/2002
Days to Decision
76 days
Submission Type
Summary

SYNTHES MIDFACE DISTRACTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022005
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/2002
Days to Decision
76 days
Submission Type
Summary