Device Classification Name |
cannula, sinus
|
510(k) Number |
K994262 |
Device Name |
FRONTAL SINUS TREPHINATION CANNULA |
Applicant |
XOMED, INC. |
6743 SOUTHPOINT DR. NORTH |
JACKSONVILLE,
FL
32216 -0980
|
|
Applicant Contact |
MARTIN D SARGENT |
Correspondent |
XOMED, INC. |
6743 SOUTHPOINT DR. NORTH |
JACKSONVILLE,
FL
32216 -0980
|
|
Correspondent Contact |
MARTIN D SARGENT |
Regulation Number | 878.4800
|
Classification Product Code |
|
Date Received | 12/17/1999 |
Decision Date | 02/08/2000 |
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
|
|
|