CLEARVIEW PLUS BONE AND VERTEBRAL BODY BIOPSY NEEDLES


Device Classification Name

instrument, biopsy

510(k) Number K022169
Device Name CLEARVIEW PLUS BONE AND VERTEBRAL BODY BIOPSY NEEDLES
Original Applicant
PARALLAX MEDICAL, INC.
940 disc dr.
scotts valley, 
CA 
95066 -4544

Original Contact richard m ruedy
Regulation Number 876.1075
Classification Product Code
KNW  
Date Received 07/03/2002
Decision Date 07/25/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Gastroenterology/Urology

510k Review Panel

General & Plastic Surgery

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No