Device Classification Name |
implant, endosseous, root-form
|
510(k) Number |
K925849 |
Device Name |
ZEST IMPLANT ANCHOR |
Applicant |
ZEST ANCHORS, INC. |
2000 M STREET, N.W. |
SUITE 700 |
WASHINGTON,
DC
20036
|
|
Applicant Contact |
DANIEL J MANELLI |
Correspondent |
ZEST ANCHORS, INC. |
2000 M STREET, N.W. |
SUITE 700 |
WASHINGTON,
DC
20036
|
|
Correspondent Contact |
DANIEL J MANELLI |
Regulation Number | 872.3640
|
Classification Product Code |
|
Date Received | 11/18/1992 |
Decision Date | 11/18/1994 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Dental
|
510k Review Panel |
Dental
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|