CADENCE SPINAL FIXATION SYSTEM


Device Classification Name

appliance, fixation, spinal interlaminal

510(k) Number K022374
Device Name CADENCE SPINAL FIXATION SYSTEM
Original Applicant
SULZER SPINE-TECH
7375 bush lake rd.
minneapolis, 
MN 
55439 -2027

Original Contact kristyn m benson
Regulation Number 888.3050
Classification Product Code
KWP  
Subsequent Product Codes
MNH   MNI  
Date Received 07/22/2002
Decision Date 09/24/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Orthopedic

510k Review Panel

Orthopedic

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No

Recalls CDRH Recalls