FDA 510(k), K142041, POROSTEON PHUSION METAL CERVICAL CAGE

FDA 510(k), K142041, POROSTEON PHUSION METAL CERVICAL CAGE

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510(K) Number: K142041
Device Name: POROSTEON PHUSION METAL CERVICAL CAGE
Manufacturer: POROSTEON, INC.
Device Classification Name: intervertebral fusion device with bone graft, cervical
Regulation Number: 888.3080
Classification Product Code: ODP
Date Received: 07/28/2014
Decision Date: 12/19/2014
Regulation Medical Specialty: Orthopedic

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