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FORTRESS™ Radiopaque Bone Cement (FORTRESS™ and FORTRESS-Plus™), CREO® Fenestrated Screw System, REVLOK® Fenestrated Screw System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172269
510(k) Type
Traditional
Applicant
Globus Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/2018
Days to Decision
242 days
Submission Type
Summary

FORTRESS™ Radiopaque Bone Cement (FORTRESS™ and FORTRESS-Plus™), CREO® Fenestrated Screw System, REVLOK® Fenestrated Screw System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172269
510(k) Type
Traditional
Applicant
Globus Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/2018
Days to Decision
242 days
Submission Type
Summary