INTERPORE CROSS INTERNATIONAL ANTERIOR FIXATION DEVICE (AFD)


Device Classification Name

spinal vertebral body replacement device

510(k) Number K022143
Device Name INTERPORE CROSS INTERNATIONAL ANTERIOR FIXATION DEVICE (AFD)
Original Applicant
INTERPORE CROSS INTL.
181 technology dr.
irvine, 
CA 
92618 -2402

Original Contact lynn m rodarti
Regulation Number 888.3060
Classification Product Code
MQP  
Date Received 07/02/2002
Decision Date 01/23/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Orthopedic

510k Review Panel

Orthopedic

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No