FDA 510(k) Applications Submitted by Marc Litzenberg
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K220331 |
02/04/2022 |
091 Balloon Guide Catheter |
InNeuroCo Inc. |
| K190338 |
02/14/2019 |
046 Zenith Flex |
InNeuroCo, Inc |
| K161262 |
05/05/2016 |
Super Distal Access (SDA) |
INNEUROCO, INC |
| K181354 |
05/22/2018 |
074 Zenith Flex System |
InNeuroCo Inc. |
| K231629 |
06/05/2023 |
091 Balloon Guide Catheter |
EOSolutions, Corp. |
| K171672 |
06/06/2017 |
065 Zenith, 074 Zenith |
InNeuroCo, Inc |
| K172167 |
07/18/2017 |
Zenith Flex System |
InNeuroCo, Inc. |
| K232260 |
07/31/2023 |
Thinline Sheath Introducer |
Inneuroco Inc. |
| K172468 |
08/15/2017 |
091 Long Sheath, 70 cm, 091 Long Sheath, 80 cm, 091 Long Sheath, 90 cm |
InNeuroCo, Inc |
| K173709 |
12/04/2017 |
Zenith Support, 95 cm, Zenith Support, 105 cm, Zenith Support, 115 cm |
InNeuroCo, Inc |
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