RIB LINK™ Fixation System

FDA 510(k) K252166 · Globus Medical, Inc.

Substantially Equivalent

510(k) numberK252166

Submission

Device name
RIB LINK™ Fixation System
Applicant
Globus Medical, Inc.
Audubon, PA, US
Received
July 10, 2025
Decision date
February 26, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HRS – Plate, Fixation, Bone
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3030
Specialty
Orthopedic
Implant
Yes

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Questions and answers

When was RIB LINK™ Fixation System cleared by the FDA?

RIB LINK™ Fixation System (K252166) received a 510(k) decision of Substantially Equivalent on February 26, 2026, 231 days after the submission was received.

What is the product code of K252166?

The FDA product code is HRS – Plate, Fixation, Bone, a Class II (moderate risk) device regulated under 21 CFR 888.3030.