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FDA 510(k) K030554, CALLOS, by Skeletal Kinetics, LLC

FDA 510(k) K030554, CALLOS, by Skeletal Kinetics, LLC

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510(K) Number: K030554
Device Name: CALLOS
Manufacturer: Skeletal Kinetics, LLC
Device Classification Name: filler, bone void, calcium compound
Regulation Number: 888.3045
Classification Product Code: MQV
Date Received: 02/21/2003
Decision Date: 05/20/2003
Regulation Medical Specialty: Orthopedic
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