Plug-Lok Cement Restirctor

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K791125 ↗

FDA Product Code

LZN

Device Class

Class II

Regulation

21 CFR Part 878.3300

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

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• Reuter Bobbin Ventila. Tube-Titanium

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• Pullen Plastic-Pore Plugs

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• Spectron Protrusio Cup

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  FDA 510(k) K823725 Active Cleared 21 Jan 1983

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