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NuVasive MLX-Medial Lateral Expandable Lumbar Interbody System, NuVasive AP Expandable XLIF System

Page Type
Cleared 510(K)
510(k) Number
K151374
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/2015
Days to Decision
76 days
Submission Type
Summary

NuVasive MLX-Medial Lateral Expandable Lumbar Interbody System, NuVasive AP Expandable XLIF System

Page Type
Cleared 510(K)
510(k) Number
K151374
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/2015
Days to Decision
76 days
Submission Type
Summary