FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
WOLF Thrombectomy System, 6F
K Number: K210530
·
Decision Aug 27, 2021
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
140
Applicant Total
5
Review Days
184
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Basic Information
- Device Name
- WOLF Thrombectomy System, 6F
- K Number
- K210530
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.5150
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Devoro Medical, Inc.
- Date Received
- February 24, 2021
- Decision Date
- August 27, 2021
- Product Code
- QEW
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| QEW | Peripheral Mechanical Thrombectomy With Aspiration | FDA class 2 | Cardiovascular |
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Other Clearances by Devoro Medical, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K241207 | SmartClaw Thrombectomy Catheter, 20 mm (FD0660-01), SmartClaw Thrombectomy Catheter, 32 mm (FD0660-02) | May 29, 2024 | Substantially Equivalent |
| K221391 | WOLF Thrombectomy SmartClaw Catheter | Nov 10, 2022 | Substantially Equivalent |
| K210911 | WOLF Thrombectomy System, 14F | Oct 19, 2021 | Substantially Equivalent |
| K200101 | WOLF Thrombectomy V System | Apr 27, 2020 | Substantially Equivalent |