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Altus Spine Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K182406
510(k) Type
Traditional
Applicant
Altus Partners, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/2019
Days to Decision
171 days
Submission Type
Summary

Altus Spine Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K182406
510(k) Type
Traditional
Applicant
Altus Partners, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/2019
Days to Decision
171 days
Submission Type
Summary