SYNTHES CERVIFIX/ AXON


Device Classification Name

appliance, fixation, spinal interlaminal

510(k) Number K023675
Device Name SYNTHES CERVIFIX/ AXON
Original Applicant
SYNTHES (USA)
1690 russell rd.
paoli, 
PA 
19301

Original Contact vikki m hoffman
Regulation Number 888.3050
Classification Product Code
KWP  
Date Received 11/01/2002
Decision Date 11/26/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Orthopedic

510k Review Panel

Orthopedic

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No