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PERIMETER Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K160418
510(k) Type
Special
Applicant
Medtronic Sofamor Danek USA, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2016
Days to Decision
20 days
Submission Type
Summary

PERIMETER Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K160418
510(k) Type
Special
Applicant
Medtronic Sofamor Danek USA, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2016
Days to Decision
20 days
Submission Type
Summary