Last synced on 18 April 2025 at 11:05 pm

ANTHEM Fracture System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173166
510(k) Type
Traditional
Applicant
Globus Medical Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2017
Days to Decision
45 days
Submission Type
Summary

ANTHEM Fracture System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173166
510(k) Type
Traditional
Applicant
Globus Medical Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2017
Days to Decision
45 days
Submission Type
Summary