Excelsius3D

by Globus Medical, Inc.

510(k) K210912

Excelsius3D is a Class II device made by Globus Medical, Inc., cleared under FDA 510(k) K210912 on 12 Aug 2021, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K210912↗

FDA record

Trust

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK210912	Date12 Aug 2021Cleared	StatusActive

Official records

FDA 510(k) database 510(k) number K210912

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number: K210912
FDA product code: OWB

Device class: Class II
Regulation: 21 CFR Part 892.1650
Advisory committee: Radiology
FDA decision: SESE Substantially Equivalent

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