Last synced on 14 November 2025 at 11:06 pm

REFIX INTERNAL FRACTURE FIXATION SCREWS

Page Type
Cleared 510(K)
510(k) Number
K050388
510(k) Type
Traditional
Applicant
XTREMI-T, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/7/2005
Days to Decision
204 days
Submission Type
Summary

REFIX INTERNAL FRACTURE FIXATION SCREWS

Page Type
Cleared 510(K)
510(k) Number
K050388
510(k) Type
Traditional
Applicant
XTREMI-T, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/7/2005
Days to Decision
204 days
Submission Type
Summary