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PERIMETER Interbody Fusion Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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