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Altus Spine Interbody Standalone Fusion System

Page Type
Cleared 510(K)
510(k) Number
K211837
510(k) Type
Traditional
Applicant
Altus Partners, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2022
Days to Decision
309 days
Submission Type
Summary

Altus Spine Interbody Standalone Fusion System

Page Type
Cleared 510(K)
510(k) Number
K211837
510(k) Type
Traditional
Applicant
Altus Partners, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2022
Days to Decision
309 days
Submission Type
Summary