Last synced on 25 April 2025 at 11:05 pm

VERSITOMIC ACL FLEXIBLE REAMER SYSTEM STERILIZATION TRAY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100887
510(k) Type
Traditional
Applicant
T.A.G. MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/2010
Days to Decision
132 days
Submission Type
Summary

VERSITOMIC ACL FLEXIBLE REAMER SYSTEM STERILIZATION TRAY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100887
510(k) Type
Traditional
Applicant
T.A.G. MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/2010
Days to Decision
132 days
Submission Type
Summary