PENTABORN


Device Classification Name

implant, endosseous, root-form

510(k) Number K072447
Device Name PENTABORN
Applicant
MEDISCITEC INC.
13 red fox lane
littleton, 
CO 
80127

Applicant Contact kevin walls
Correspondent
MEDISCITEC INC.
13 red fox lane
littleton, 
CO 
80127

Correspodent Contact kevin walls
Regulation Number 872.3640
Classification Product Code
DZE  
Date Received 08/31/2007
Decision Date 02/15/2008
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Dental

510k Review Panel

Dental

Type Traditional
Reviewed by Third Party No

Combination Product

No