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VariLift-LX Interbody Fusion System, VariLift-C Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K180822
510(k) Type
Traditional
Applicant
Wenzel Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/2019
Days to Decision
304 days
Submission Type
Summary

VariLift-LX Interbody Fusion System, VariLift-C Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K180822
510(k) Type
Traditional
Applicant
Wenzel Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/2019
Days to Decision
304 days
Submission Type
Summary