FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

WOLF Thrombectomy System, 14F

K Number: K210911 · Decision Oct 19, 2021
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
140
Applicant Total
5
Review Days
204

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Basic Information

Device Name
WOLF Thrombectomy System, 14F
K Number
K210911
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
March 29, 2021
Decision Date
October 19, 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
QEW Peripheral Mechanical Thrombectomy With Aspiration

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (QEW), ordered by most recent decision date.

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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)
K221391 WOLF Thrombectomy™ SmartClaw Catheter
K210530 WOLF Thrombectomy System, 6F
K200101 WOLF Thrombectomy V System