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VARILIFT-L INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K131296
510(k) Type
Traditional
Applicant
WENZEL SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/2013
Days to Decision
120 days
Submission Type
Summary

VARILIFT-L INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K131296
510(k) Type
Traditional
Applicant
WENZEL SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/2013
Days to Decision
120 days
Submission Type
Summary