Nexpowder
FDA 510(k) K240994 · Nextbiomedical Co., Ltd.
510(k) numberK240994
Submission
- Device name
- Nexpowder
- Applicant
- Nextbiomedical Co., Ltd.
Incheon, KR - Received
- April 11, 2024
- Decision date
- November 27, 2024
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- QAU – Hemostatic Device For Endoscopic Gastrointestinal Use
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.4456
- Specialty
- General, Plastic Surgery
- Implant
- Yes
Hemostatic device for intraluminal gastrointestinal use. A hemostatic device for intraluminal gastrointestinal use is a prescription device that is endoscopically applied to the upper and/or lower gastrointestinal tract and is intended to produce hemostasis via absorption of fluid or by other physical means.
Other 510(k)s with product code QAU
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K261503 | PuraStat GIQAU · Traditional | 3-D Matrix, Inc. | 08/03/2026SE |
| K253302 | Hemospray Endoscopic Hemostat (HEMO-[X])QAU · Traditional | Wilson-Cook Medical, Inc. | 06/02/2026SE |
| K253924 | PuraStatQAU · Special | 3-D Matrix Europe SAS | 01/07/2026SE |
| K242250 | PuraStatQAU · Traditional | 3-D Matrix Europe SAS | 10/22/2024SE |
| K234131 | Resolv Endoscopic Hemostat SystemQAU · Traditional | Hemostasis, LLC | 07/26/2024SE |
| K222481 | PuraStatQAU · Traditional | 3-D Matrix, Inc. | 02/28/2023SE |
| K202929 | NexpowderQAU · Traditional | Nextbiomedical Co., Ltd. | 09/16/2022SE |
| K210098 | PuraStat-GIQAU · Traditional | 3-D Matrix, Inc. | 06/25/2021SE |
| K190677 | EndoClotQAU · Traditional | Endoclot Plus Co., Ltd. | 01/29/2021SE |
| K200972 | Hemospray Endoscopic HemostatQAU · Traditional | Wilson-Cook Medical, Inc. | 06/10/2020SE |
More from Wilson-Cook Medical, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K202929 | NexpowderQAU · Traditional | 09/16/2022SE |
Questions and answers
When was Nexpowder cleared by the FDA?
Nexpowder (K240994) received a 510(k) decision of Substantially Equivalent on November 27, 2024, 230 days after the submission was received.
What is the product code of K240994?
The FDA product code is QAU – Hemostatic Device For Endoscopic Gastrointestinal Use, a Class II (moderate risk) device regulated under 21 CFR 878.4456.