Last synced on 23 May 2025 at 11:06 pm

SYNTHES PATIENT SPECIFIC PLATE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122647
510(k) Type
Traditional
Applicant
SYNTHES INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2013
Days to Decision
182 days
Submission Type
Summary

SYNTHES PATIENT SPECIFIC PLATE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122647
510(k) Type
Traditional
Applicant
SYNTHES INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2013
Days to Decision
182 days
Submission Type
Summary