Last synced on 25 January 2026 at 3:41 am

Altus Spine Interbody Standalone Fusion System

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