Codman Hakim Programmable Valve W/Wo Siphonguard

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K053107 ↗

FDA Product Code

JXG

Device Class

Class II

Regulation

21 CFR Part 882.5550

Advisory Committee

Neurology

FDA Decision

SESE Substantially Equivalent

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See all devices from Codman & Shurtleff, Inc. →