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VariLift-L Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K151900
510(k) Type
Traditional
Applicant
WENZEL SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/2015
Days to Decision
154 days
Submission Type
Summary

VariLift-L Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K151900
510(k) Type
Traditional
Applicant
WENZEL SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/2015
Days to Decision
154 days
Submission Type
Summary