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VariLift®-C Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K231076
510(k) Type
Traditional
Applicant
Wenzel Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/2023
Days to Decision
166 days
Submission Type
Summary

VariLift®-C Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K231076
510(k) Type
Traditional
Applicant
Wenzel Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/2023
Days to Decision
166 days
Submission Type
Summary