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TIMESH SELF DRILLING SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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