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NuVasive® MLX® – Medial Lateral Expandable Lumbar Interbody System; NuVasive® AP Expandable XLIF System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173025
510(k) Type
Traditional
Applicant
Nu Vasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/2018
Days to Decision
133 days
Submission Type
Summary

NuVasive® MLX® – Medial Lateral Expandable Lumbar Interbody System; NuVasive® AP Expandable XLIF System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173025
510(k) Type
Traditional
Applicant
Nu Vasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/2018
Days to Decision
133 days
Submission Type
Summary