Osteobridge Ika Intramedullary Knee Arthrodesis Rod Fixation System

• • Terminated Z-0435-2021 FDA Class II ·initiated 18 Sep 2020

  Product may be mislabeled.

510(k) Number

K101939 ↗

FDA Product Code

HSB

Device Class

Class II

Regulation

21 CFR Part 888.3020

Advisory Committee

Orthopedic

FDA Decision

SESE Substantially Equivalent

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• Metafix Blp Plate, Size 31, Left, Metafix Blp Plate, Size 31, Right

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• Merete Locking Bone Plate System III

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• Merete Locking Bone Plate System

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• OsteoBridge IDSF - Intramedullary Diaphyseal Segmental Defect Fixation Rod System

  Class II

  FDA 510(k) K142451 Active Cleared 9 Feb 2015

See all devices from Merete Medical GmbH →