Spectron Conversion Endoprosthesis Cup

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K823726 ↗

FDA Product Code

KWY

Device Class

Class II

Regulation

21 CFR Part 888.3390

Advisory Committee

Orthopedic

FDA Decision

SESE Substantially Equivalent

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See all devices from Richard'S Medical Equip., Inc. →