Last synced on 12 October 2025 at 8:21 pm

PRO FIXATION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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