Device Classification Name |
bone grafting material, synthetic
|
510(k) Number |
K840260 |
Device Name |
PERIOGRAF DURAPATITE 40-60 MESH |
Applicant |
STERLING DRUG, INC. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Correspondent |
STERLING DRUG, INC. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Regulation Number | 872.3930
|
Classification Product Code |
|
Date Received | 01/10/1984 |
Decision Date | 04/05/1984 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Dental
|
510k Review Panel |
Dental
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|