| Device Classification Name |
Abutment, Implant, Dental, Endosseous
More FDA Info for this Device |
| 510(K) Number |
K021460 |
| Device Name |
Abutment, Implant, Dental, Endosseous |
| Applicant |
"O" CO., INC.
600 PAISANO, N.E., SUITE A
ALBUQUERQUE, NM 87123 US
Other 510(k) Applications for this Company
|
| Contact |
DAVID D DALISE
Other 510(k) Applications for this Contact |
| Regulation Number |
872.3630
More FDA Info for this Regulation Number |
| Classification Product Code |
NHA
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
| Date Received |
05/07/2002 |
| Decision Date |
05/22/2002 |
| Decision |
SESE - SUBST EQUIV |
| Classification Advisory Committee |
DE - Dental |
| Review Advisory Committee |
DE - Dental |
| Statement / Summary / Purged Status |
Statement |
| Type |
Special |
| Reviewed By Third Party |
N |
| Expedited Review |
|