Device Classification Name |
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
More FDA Info for this Device |
510(K) Number |
K953202 |
Device Name |
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented |
Applicant |
JOHNSON & JOHNSON PROFESSIONALS, INC.
325 PARAMOUNT DR.
RAYNHAM, MA 02767-0350 US
Other 510(k) Applications for this Company
|
Contact |
J. TERESA DORRIETY
Other 510(k) Applications for this Contact |
Regulation Number |
888.3350
More FDA Info for this Regulation Number |
Classification Product Code |
JDI
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
07/10/1995 |
Decision Date |
01/31/1996 |
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 |
|