CTXA HIP; CTXA; QCT PRO CTXA HIP


Device Classification Name

densitometer, bone

510(k) Number K002113
Device Name CTXA HIP; CTXA; QCT PRO CTXA HIP
Original Applicant
MINDWAYS SOFTWARE, INC.
282 second st., 4th fl.
san francisco, 
CA 
94105 -3130

Original Contact christopher cann
Regulation Number 892.1170
Classification Product Code
KGI  
Date Received 06/07/2000
Decision Date 12/04/2001
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Radiology

510k Review Panel

Radiology

Type Traditional
Reviewed by Third Party No

Combination Product

No