Device Classification Name |
Prosthesis, Knee Patellofemorotibial, Partial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
More FDA Info for this Device |
510(K) Number |
K061648 |
Device Name |
Prosthesis, Knee Patellofemorotibial, Partial, Semi-Constrained, Cemented, Polymer/Metal/Polymer |
Applicant |
DEPUY ORTHOPAEDICS, INC.
P.O. BOX 988
WARSAW, IN 46581-0988 US
Other 510(k) Applications for this Company
|
Contact |
NANCY FRIDDLE
Other 510(k) Applications for this Contact |
Regulation Number |
888.3560
More FDA Info for this Regulation Number |
Classification Product Code |
NPJ
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
06/13/2006 |
Decision Date |
09/11/2006 |
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 |
|