Class Class II

G7® Revision Acetabular System (K252623)

K252623 2026-02-04 Traditional
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Description

G7® Revision Acetabular System by Zimmer, Inc., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252623
Clearance Date2026-02-04
Clearance TypeTraditional
Product CodeLPH
Regulation Number888.3358

Categories

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