Device Classification Name |
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
More FDA Info for this Device |
510(K) Number |
K960856 |
Device Name |
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer |
Applicant |
BIOMET, INC.
AIRPORT INDUSTRIAL PARK,
P.O.BOX 587
WARSAW, IN 46581-0587 US
Other 510(k) Applications for this Company
|
Contact |
MARY L VERSTYNEN
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 |
03/01/1996 |
Decision Date |
11/27/1996 |
Decision |
SN - Substantially Equivalent for Some Indications |
Classification Advisory Committee |
OR - Orthopedic |
Review Advisory Committee |
OR - Orthopedic |
Statement / Summary / Purged Status |
|
Type |
Traditional |
Reviewed By Third Party |
N |
Expedited Review |
|