LEFORTE SYSTEM BONE PLATE


Device Classification Name

appliance, fixation, nail/blade/plate combination, single component

510(k) Number K023360
Device Name LEFORTE SYSTEM BONE PLATE
Original Applicant
JEIL MEDICAL CORPORATION
po box 7007
deerfiled, 
IL 
60015

Original Contact daniel kamm
Regulation Number 888.3030
Classification Product Code
KTW  
Date Received 10/07/2002
Decision Date 10/25/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Orthopedic

510k Review Panel

Orthopedic

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No