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Modulift Vertebral Body Replacement (VBR) System

Page Type
Cleared 510(K)
510(k) Number
K172032
510(k) Type
Traditional
Applicant
Aesculap Implants Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2017
Days to Decision
138 days
Submission Type
Summary

Modulift Vertebral Body Replacement (VBR) System

Page Type
Cleared 510(K)
510(k) Number
K172032
510(k) Type
Traditional
Applicant
Aesculap Implants Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2017
Days to Decision
138 days
Submission Type
Summary