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 |
|