Duracon Unicompartmental Knee System

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K926231 ↗

FDA Product Code

HSX

Device Class

Class II

Regulation

21 CFR Part 888.3520

Advisory Committee

Orthopedic

FDA Decision

SESE Substantially Equivalent

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• Alta Femoral Intramedullary Rods/Cfx Rods Modification

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• Naso-Gard Nasogastric Tube Holder

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• Class of Casting Alloys Type III or Alt

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• Howmedica Zirconia Ceramic Femoral Head

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• Extended Balljoint Grip

  Class II

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See all devices from Howmedica Corp. →