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ANTHEM™ Fracture System

Page Type
Cleared 510(K)
510(k) Number
K163361
510(k) Type
Traditional
Applicant
Globus Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2017
Days to Decision
128 days
Submission Type
Summary

ANTHEM™ Fracture System

Page Type
Cleared 510(K)
510(k) Number
K163361
510(k) Type
Traditional
Applicant
Globus Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2017
Days to Decision
128 days
Submission Type
Summary