FDA 510(k), K072764, KLS MARTIN XTERNAL FIXATOR

FDA 510(k), K072764, KLS MARTIN XTERNAL FIXATOR

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510(K) Number: K072764
Device Name: KLS MARTIN XTERNAL FIXATOR
Manufacturer: KLS MARTIN L.P.
Device Classification Name: external mandibular fixator and/or distractor
Regulation Number: 872.4760
Classification Product Code: MQN
Date Received: 09/28/2007
Decision Date: 12/20/2007
Regulation Medical Specialty: Dental

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