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FDA 510(k), K012305, MODIFICATION TO: TRINICA ANTERIOR CERVICAL PLATE SYSTEM
FDA 510(k), K012305, MODIFICATION TO: TRINICA ANTERIOR CERVICAL PLATE SYSTEM
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510(K) Number: K012305
Device Name: MODIFICATION TO: TRINICA ANTERIOR CERVICAL PLATE SYSTEM
Manufacturer: SULZER SPINE-TECH
Device Classification Name: appliance, fixation, spinal intervertebral body
Regulation Number: 888.3060
Classification Product Code: KWQ
Date Received: 07/23/2001
Decision Date: 08/22/2001
Regulation Medical Specialty: Orthopedic
Device Name: MODIFICATION TO: TRINICA ANTERIOR CERVICAL PLATE SYSTEM
Manufacturer: SULZER SPINE-TECH
Device Classification Name: appliance, fixation, spinal intervertebral body
Regulation Number: 888.3060
Classification Product Code: KWQ
Date Received: 07/23/2001
Decision Date: 08/22/2001
Regulation Medical Specialty: Orthopedic
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