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Altus Spine Titanium Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K171329
510(k) Type
Special
Applicant
Altus Partners, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2017
Days to Decision
116 days
Submission Type
Summary

Altus Spine Titanium Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K171329
510(k) Type
Special
Applicant
Altus Partners, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2017
Days to Decision
116 days
Submission Type
Summary