Codman Anterior Cervical Spine Plate System

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K934756 ↗

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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  FDA 510(k) K902257 Active Cleared 19 Jul 1990

• Orbit Galaxy G2 Microcoil Delivery System

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See all devices from Codman & Shurtleff, Inc. →