ENDIUS ATAVI SYSTEM


Device Classification Name

arthroscope

510(k) Number K021748
Device Name ENDIUS ATAVI SYSTEM
Original Applicant
ENDIUS, INC.
23 west bacon st.
plainville, 
MA 
02762

Original Contact christine kuntz-nassif
Regulation Number 888.1100
Classification Product Code
HRX  
Date Received 05/28/2002
Decision Date 06/26/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Orthopedic

510k Review Panel

General & Plastic Surgery

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No