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INERTIA® CONNEXX™ Modular Pedicle Screw System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231799
510(k) Type
Special
Applicant
Nexxt Spine LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2023
Days to Decision
30 days
Submission Type
Summary

INERTIA® CONNEXX™ Modular Pedicle Screw System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231799
510(k) Type
Special
Applicant
Nexxt Spine LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2023
Days to Decision
30 days
Submission Type
Summary