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PERIMETER INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K131669
510(k) Type
Traditional
Applicant
MEDTRONIC SOFAMOR DANEK USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/2013
Days to Decision
147 days
Submission Type
Summary

PERIMETER INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K131669
510(k) Type
Traditional
Applicant
MEDTRONIC SOFAMOR DANEK USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/2013
Days to Decision
147 days
Submission Type
Summary