510(k) K230565

Device
HILINE? Fixation System
Applicant
Globus Medical, Inc.
510(k) number
K230565
Product code
OWI
Decision
Substantially Equivalent (SESE)
Decision date
2023-04-20
Date received
2023-03-01
Regulation
888.3010
Classification name
Bone Fixation Cerclage, Sublaminar
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Jennifer Antonacci
Address
2560 General Armistead Ave. Audubon PA US 19403 19403

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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