Last synced on 6 December 2024 at 11:05 pm

SYNTHES ORTHODONTIC BONE ANCHOR SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093299
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2010
Days to Decision
421 days
Submission Type
Summary

SYNTHES ORTHODONTIC BONE ANCHOR SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093299
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2010
Days to Decision
421 days
Submission Type
Summary