Last synced on 14 November 2025 at 11:06 pm

TIMESH SELF DRILLING SCREW

Page Type
Cleared 510(K)
510(k) Number
K062348
510(k) Type
Special
Applicant
MEDTRONIC NEUROSURGERY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/2006
Days to Decision
28 days
Submission Type
Summary

TIMESH SELF DRILLING SCREW

Page Type
Cleared 510(K)
510(k) Number
K062348
510(k) Type
Special
Applicant
MEDTRONIC NEUROSURGERY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/2006
Days to Decision
28 days
Submission Type
Summary