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Parker Quality & Compliance

PQC Reg Watch

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Device type

Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Trunnion-Bearing

Product code LGE · Class II · 21 CFR 888.3530 · Orthopedic

FDA classification database

Recent 510(k)s

No 510(k) clearances in the archive for LGE.

Recent recalls