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Altus Spine HA Pedicle Screw System

Page Type
Cleared 510(K)
510(k) Number
K200922
510(k) Type
Special
Applicant
Altus Partners, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/2021
Days to Decision
295 days
Submission Type
Summary

Altus Spine HA Pedicle Screw System

Page Type
Cleared 510(K)
510(k) Number
K200922
510(k) Type
Special
Applicant
Altus Partners, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/2021
Days to Decision
295 days
Submission Type
Summary