LITe Plate System

by Stryker Corporation

510(k) K142699

LITe Plate System is a Class II device made by Stryker Corporation.

Listed No authorization on record

Valid until

Not applicable

No authorization on record

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source FDA 510(k), synced 1 Jun 2026.

Specification

510(k)

510(k) Number: K142699
FDA product code: KWQ

Device class: Class II
Regulation: 21 CFR Part 888.3060
Advisory committee: Orthopedic
FDA decision: SESE Substantially Equivalent

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