SENOJ IMPLANT SYSTEM


Device Classification Name

implant, endosseous, root-form

510(k) Number K000889
Device Name SENOJ IMPLANT SYSTEM
Original Applicant
SENOJ BIOCARE, INC.
8910 university center ln.
suite 265
san diego, 
CA 
92122 -1085

Original Contact penny wollum
Regulation Number 872.3640
Classification Product Code
DZE  
Date Received 03/20/2000
Decision Date 04/27/2001
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Dental

510k Review Panel

Dental

Type Traditional
Reviewed by Third Party No

Combination Product

No