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Leva® Anterior Interbody System

Page Type
Cleared 510(K)
510(k) Number
K161993
510(k) Type
Traditional
Applicant
Spine Wave, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/2016
Days to Decision
126 days
Submission Type
Summary

Leva® Anterior Interbody System

Page Type
Cleared 510(K)
510(k) Number
K161993
510(k) Type
Traditional
Applicant
Spine Wave, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/2016
Days to Decision
126 days
Submission Type
Summary