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MR8 Drill System

Page Type
Cleared 510(K)
510(k) Number
K163565
510(k) Type
Traditional
Applicant
MEDTRONIC POWERED SURGICAL SOLUTIONS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2017
Days to Decision
99 days
Submission Type
Summary

MR8 Drill System

Page Type
Cleared 510(K)
510(k) Number
K163565
510(k) Type
Traditional
Applicant
MEDTRONIC POWERED SURGICAL SOLUTIONS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2017
Days to Decision
99 days
Submission Type
Summary