Device Classification Name |
Prosthesis, Knee, Hemi-, Tibial, Resurfacing (Uncemented)
More FDA Info for this Device |
510(K) Number |
K022779 |
Device Name |
Prosthesis, Knee, Hemi-, Tibial, Resurfacing (Uncemented) |
Applicant |
OSTEOIMPLANT TECHNOLOGY, INC.
11201 PEPPER RD.
HUNT VALLEY, MD 21031-1201 US
Other 510(k) Applications for this Company
|
Contact |
SAM SON
Other 510(k) Applications for this Contact |
Regulation Number |
888.3590
More FDA Info for this Regulation Number |
Classification Product Code |
HSH
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
08/22/2002 |
Decision Date |
11/20/2002 |
Decision |
SESE - SUBST EQUIV |
Classification Advisory Committee |
OR - Orthopedic |
Review Advisory Committee |
OR - Orthopedic |
Statement / Summary / Purged Status |
Statement |
Type |
Traditional |
Reviewed By Third Party |
N |
Expedited Review |
|