LEFORTE SYSTEM BONE SCREW


Device Classification Name

screw, fixation, bone

510(k) Number K023365
Device Name LEFORTE SYSTEM BONE SCREW
Original Applicant
JEIL MEDICAL CORPORATION
po box 7007
deerfiled, 
IL 
60015

Original Contact daniel kamm
Regulation Number 888.3040
Classification Product Code
HWC  
Date Received 10/07/2002
Decision Date 04/18/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Orthopedic

510k Review Panel

Orthopedic

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No