Hall Modular Acetabular Reamer System

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K960852 ↗

FDA Product Code

HWE

Device Class

Class I

Regulation

21 CFR Part 878.4820

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

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  Class II

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