Device Classification Name |
prosthesis, hip, femoral, resurfacing
|
510(k) Number |
K904870 |
Device Name |
MODIFIED NEW JERSEY FEMORAL HIP RESURFACING COMPON |
Applicant |
ENDOTEC, INC. |
20 VALLEY ST. |
SOUTH ORANGE,
NJ
07079
|
|
Applicant Contact |
MICHAEL J PAPPAS |
Correspondent |
ENDOTEC, INC. |
20 VALLEY ST. |
SOUTH ORANGE,
NJ
07079
|
|
Correspondent Contact |
MICHAEL J PAPPAS |
Regulation Number | 888.3400
|
Classification Product Code |
|
Date Received | 10/23/1990 |
Decision Date | 05/23/1991 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Orthopedic
|
510k Review Panel |
Orthopedic
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
Recalls |
CDRH Recalls
|
|
|