Device Classification Name |
electrosurgical, cutting & coagulation & accessories
|
510(k) Number |
K232033 |
Device Name |
HYBRIDknife® flex |
Applicant |
Erbe Elektromedizin GmbH |
Waldhoernlestrasse 17 |
Tuebingen,
DE
72072
|
|
Applicant Contact |
Matthias Kollek |
Correspondent |
Erbe Elektromedizin GmbH |
Waldhoernlestrasse 17 |
Tuebingen,
DE
72072
|
|
Correspondent Contact |
Matthias Kollek |
Regulation Number | 878.4400
|
Classification Product Code |
|
Subsequent Product Code |
|
Date Received | 07/07/2023 |
Decision Date | 11/29/2023 |
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
|