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FDA 510(k) K122801, PROVIDENCE CERVICAL CAGE, by Providence Medical Technology, Inc.

FDA 510(k) K122801, PROVIDENCE CERVICAL CAGE, by Providence Medical Technology, Inc.

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510(K) Number: K122801
Device Name: PROVIDENCE CERVICAL CAGE
Manufacturer: Providence Medical Technology, Inc.
Device Classification Name: intervertebral fusion device with bone graft, cervical
Regulation Number: 888.3080
Classification Product Code: ODP
Date Received: 09/13/2012
Decision Date: 05/24/2013
Regulation Medical Specialty: Orthopedic

Total pages: 531
Fully redacted pages: 198
Content pages: 333

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