Device Classification Name |
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
More FDA Info for this Device |
510(K) Number |
K071499 |
Device Name |
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer |
Applicant |
AESCULAP IMPLANT SYSTEMS, INC.
3773 CORPORATE PKWY.
CENTER VALLEY, PA 18034 US
Other 510(k) Applications for this Company
|
Contact |
KATHY A RACOSKY
Other 510(k) Applications for this Contact |
Regulation Number |
888.3560
More FDA Info for this Regulation Number |
Classification Product Code |
JWH
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
05/31/2007 |
Decision Date |
09/14/2007 |
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 |
|