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MLX™ - Medial Lateral Expandable Lumbar Interbody System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K153105
510(k) Type
Traditional
Applicant
Nu Vasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/2016
Days to Decision
258 days
Submission Type
Summary

MLX™ - Medial Lateral Expandable Lumbar Interbody System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K153105
510(k) Type
Traditional
Applicant
Nu Vasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/2016
Days to Decision
258 days
Submission Type
Summary