Last synced on 20 December 2024 at 11:05 pm

U-CLIP DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062821
510(k) Type
Traditional
Applicant
MEDTRONIC NEUROSURGERY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/2006
Days to Decision
90 days
Submission Type
Summary

U-CLIP DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062821
510(k) Type
Traditional
Applicant
MEDTRONIC NEUROSURGERY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/2006
Days to Decision
90 days
Submission Type
Summary