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Navigated Anterolateral Disc Prep Instruments

Page Type
Cleared 510(K)
510(k) Number
K211441
510(k) Type
Special
Applicant
Medtronic Sofamor Danek USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/9/2021
Days to Decision
30 days
Submission Type
Summary

Navigated Anterolateral Disc Prep Instruments

Page Type
Cleared 510(K)
510(k) Number
K211441
510(k) Type
Special
Applicant
Medtronic Sofamor Danek USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/9/2021
Days to Decision
30 days
Submission Type
Summary