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CORNERSTONE PSR CERVICAL INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K100214
510(k) Type
Traditional
Applicant
Medtronic Sofamor Danek
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/25/2010
Days to Decision
151 days
Submission Type
Summary

CORNERSTONE PSR CERVICAL INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K100214
510(k) Type
Traditional
Applicant
Medtronic Sofamor Danek
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/25/2010
Days to Decision
151 days
Submission Type
Summary