Mercury Spinal System

by Spinal Elements, Inc. 6 variants

510(k) K141372

Mercury Spinal System is a Class II device made by Spinal Elements, Inc., cleared under FDA 510(k) K141372 on 22 Aug 2014, 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) K141372↗

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	NumberK141372	Date22 Aug 2014Cleared	StatusActive

Official records

FDA 510(k) database 510(k) number K141372

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number: K141372
FDA product code: NKB

Device class: Class II
Regulation: 21 CFR Part 888.3070
Advisory committee: Orthopedic
FDA decision: SESE Substantially Equivalent

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