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FDA 510(k), K030327, ZEPHIR ANTERIOR CERVICAL SYSTEM
FDA 510(k), K030327, ZEPHIR ANTERIOR CERVICAL SYSTEM
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510(K) Number: K030327
Device Name: ZEPHIR ANTERIOR CERVICAL SYSTEM
Manufacturer: RICHARD TREHARNE
Device Classification Name: Appliance, Fixation, Spinal Intervertebral Body
Regulation Number: KWQ
Classification Product Code: KXA
Date Received: 01/31/2003
Decision Date: 02/26/2003
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
Device Name: ZEPHIR ANTERIOR CERVICAL SYSTEM
Manufacturer: RICHARD TREHARNE
Device Classification Name: Appliance, Fixation, Spinal Intervertebral Body
Regulation Number: KWQ
Classification Product Code: KXA
Date Received: 01/31/2003
Decision Date: 02/26/2003
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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