Last synced on 25 January 2026 at 3:41 am

PRO FIXATION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110538
510(k) Type
Traditional
Applicant
Synovis Orthopedic & Woundcare
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/2011
Days to Decision
137 days
Submission Type
Summary

PRO FIXATION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110538
510(k) Type
Traditional
Applicant
Synovis Orthopedic & Woundcare
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/2011
Days to Decision
137 days
Submission Type
Summary