MICROFIX QUICKANCHOR PLUS


Device Classification Name

screw, fixation, bone

510(k) Number K024115
Device Name MICROFIX QUICKANCHOR PLUS
Original Applicant
MITEK WORLDWIDE
249 vanderbilt ave.
norwood, 
MA 
02062

Original Contact ruth c forstadt
Regulation Number 888.3040
Classification Product Code
HWC  
Date Received 12/13/2002
Decision Date 03/13/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Orthopedic

510k Review Panel

Orthopedic

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No