Device Classification Name |
mesh, surgical
|
510(k) Number |
K041923 |
Device Name |
BIOBLANKET |
Applicant |
KENSEY NASH CORP. |
55 EAST UWCHLAN AVE. |
EXTON,
PA
19341
|
|
Applicant Contact |
DEBORAH RACIOPPI |
Correspondent |
KENSEY NASH CORP. |
55 EAST UWCHLAN AVE. |
EXTON,
PA
19341
|
|
Correspondent Contact |
DEBORAH RACIOPPI |
Regulation Number | 878.3300
|
Classification Product Code |
|
Date Received | 07/16/2004 |
Decision Date | 09/08/2004 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General & Plastic Surgery
|
510k Review Panel |
General & Plastic Surgery
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|