SOHNIKS


Device Classification Name

arthroscope

510(k) Number K023783
Device Name SOHNIKS
Original Applicant
SOHNIKS ENDOSCOPY, INC.
930 blue gentian rd.
suite 1400
eagan, 
MN 
55121

Original Contact marc hoskins
Regulation Number 888.1100
Classification Product Code
HRX  
Date Received 11/12/2002
Decision Date 02/07/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Orthopedic

510k Review Panel

General & Plastic Surgery

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No