DeviceClearance

CREO® Stabilization System, REVERE® Stabilization System— 510(k) K181068

Substantially Equivalent

Globus Medical, Inc.

FDA 510(k) clearance K181068 for CREO® Stabilization System, REVERE® Stabilization System, Substantially Equivalent on 2018-06-29. Applicant: Globus Medical, Inc..

Clearance details

Applicant
Globus Medical, Inc.
Product code
Code PGM
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Audubon, PA, US
Download summary PDFView on FDA.gov ↗

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