Device Classification Name |
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
More FDA Info for this Device |
510(K) Number |
K984291 |
Device Name |
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer |
Applicant |
IMPLEX CORP.
80 COMMERCE DR.
ALLENDALE, NJ 07401-1600 US
Other 510(k) Applications for this Company
|
Contact |
JOHN SCHALAGO
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 |
12/01/1998 |
Decision Date |
02/01/1999 |
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 |
|