FDASeptember 1, 2017device

The ELAN 4 Air System is intended for high speed cutting, sawing and drilling of bone in fields of Spine, ENT, Neuro, and Maxillofacial Surgery.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The ELAN 4 Air System was released to the market place prior to an authorized FDA 510K clearance. This issue does not affected sales outside the United States (OUS).

What to do

FDA enforcement status: Terminated

Brands named

aesculap implant systemsaesculapaesculap implant

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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