Last synced on 25 January 2026 at 3:41 am

ORTHOMESH

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073115
510(k) Type
Traditional
Applicant
Synthes (Usa)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2008
Days to Decision
253 days
Submission Type
Summary

ORTHOMESH

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073115
510(k) Type
Traditional
Applicant
Synthes (Usa)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2008
Days to Decision
253 days
Submission Type
Summary