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Ackermann Instrumente GmbH

3 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
Ackermann Intervertebral Body Fusion Device (K143450)Ackermann Instrumente GmbH2015-09-16
ACKERMANN EUROPCLIP (K111930)Ackermann Instrumente GmbH2011-11-08
ACKERMANN SURGICAL INSTRUMENTS (K974382)Ackermann Instrumente GmbH1998-04-21

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Every clearance here is in the API, with alerts when new ones post.