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PERIMETER INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K090353
510(k) Type
Traditional
Applicant
MEDTRONIC SOFAMOR DANEK
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/2009
Days to Decision
230 days
Submission Type
Summary

PERIMETER INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K090353
510(k) Type
Traditional
Applicant
MEDTRONIC SOFAMOR DANEK
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/2009
Days to Decision
230 days
Submission Type
Summary