INTERPORE CROSS ANTERIOR CERVICAL PLATE SYSTEM


information about

Device Classification Name

appliance, fixation, spinal intervertebral body

510(k) Number K002592
Device Name INTERPORE CROSS ANTERIOR CERVICAL PLATE SYSTEM
Original Applicant
INTERPORE CROSS INTL.
181 technology dr.
irvine, 
CA 
92618 -2402

Original Contact prosie rey-fessler
Regulation Number 888.3060
Classification Product Code
KWQ  
Date Received 08/21/2000
Decision Date 10/06/2000
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Orthopedic

510k Review Panel

Orthopedic

Type Traditional
Reviewed by Third Party No

Combination Product

No