Last synced on 14 November 2025 at 11:06 pm

Altus Spine Pedicle Screw System

Page Type
Cleared 510(K)
510(k) Number
K181339
510(k) Type
Traditional
Applicant
Altus Partners, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/2018
Days to Decision
64 days
Submission Type
Summary

Altus Spine Pedicle Screw System

Page Type
Cleared 510(K)
510(k) Number
K181339
510(k) Type
Traditional
Applicant
Altus Partners, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/2018
Days to Decision
64 days
Submission Type
Summary