Device Classification Name |
Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
More FDA Info for this Device |
510(K) Number |
K081111 |
Device Name |
Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer |
Applicant |
SMITH & NEPHEW, INC.
1450 E BROOKS ROAD
MEMPHIS, TN 38116 US
Other 510(k) Applications for this Company
|
Contact |
NICHOLAS B TABRIZI
Other 510(k) Applications for this Contact |
Regulation Number |
888.3510
More FDA Info for this Regulation Number |
Classification Product Code |
KRO
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
04/18/2008 |
Decision Date |
07/23/2008 |
Decision |
SESE - SUBST EQUIV |
Classification Advisory Committee |
OR - Orthopedic |
Review Advisory Committee |
OR - Orthopedic |
Statement / Summary / Purged Status |
Summary |
Type |
Traditional |
Reviewed By Third Party |
N |
Expedited Review |
|