RELIEVE LAMINOPLASTY FIXATION SYSTEM— 510(k) K080664

Substantially Equivalent

Globus Medical, Inc.

FDA 510(k) clearance K080664 for RELIEVE LAMINOPLASTY FIXATION SYSTEM, Substantially Equivalent on 2008-07-25. Applicant: Globus Medical, Inc..

Clearance details

Applicant: Globus Medical, Inc.
Product code: Code NQW
Advisory panel: Orthopedic
Date received: 2008-03-10
Decision date: 2008-07-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Audubon, PA, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.