Device Classification Name |
prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer
|
510(k) Number |
K924940 |
Device Name |
FEMORAL & TIBIAL AUGMENT BLOCK |
Applicant |
JOINT MEDICAL PRODUCTS CORP. |
860 CANAL ST. |
STAMFORD,
CT
06902
|
|
Applicant Contact |
DEBRA L BING |
Correspondent |
JOINT MEDICAL PRODUCTS CORP. |
860 CANAL ST. |
STAMFORD,
CT
06902
|
|
Correspondent Contact |
DEBRA L BING |
Regulation Number | 888.3560
|
Classification Product Code |
|
Date Received | 09/30/1992 |
Decision Date | 03/09/1993 |
Decision |
SUBSTANTIALLY EQUIVALENT FOR SOME INDICATIONS
(SN) |
Regulation Medical Specialty |
Orthopedic
|
510k Review Panel |
Orthopedic
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|