Device Classification Name |
Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
More FDA Info for this Device |
510(K) Number |
K982859 |
Device Name |
Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer |
Applicant |
PLUS ORTHOPEDICS
3550 GENERAL ATOMICS CT.
BLDG. 15-100
SAN DIEGO, CA 92121-1122 US
Other 510(k) Applications for this Company
|
Contact |
HARTMUT LOCH
Other 510(k) Applications for this Contact |
Regulation Number |
888.3530
More FDA Info for this Regulation Number |
Classification Product Code |
HRY
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
08/13/1998 |
Decision Date |
07/30/1999 |
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 |
|