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Modulift Vertebral Body Replacement (VBR) System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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