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

Symphony™ Thrombectomy System and Symphony™ 16F 82cm Thrombectomy System

K Number: K252057 · Decision Aug 28, 2025
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
140
Applicant Total
17
Review Days
58

Basic Information

Device Name
Symphony™ Thrombectomy System and Symphony™ 16F 82cm Thrombectomy System
K Number
K252057
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5150
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Imperative Care, Inc.
Date Received
July 1, 2025
Decision Date
August 28, 2025
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 Imperative Care, Inc.

K Number Device Name
K252046 Zoom System (Zoom 4S Catheter)
K244061 X-Wire Guidewire
K243047 Zoom 7X Catheter; Zoom Aspiration Tubing; Zoom POD Aspiration Tubing
K250775 Symphony™ Thrombectomy System; Symphony™ 16F 82cm Thrombectomy System
K242672 Zoom System
K240948 TracStar LDP Large Distal Platform; Zoom 88 Large Distal Platform; Zoom 88 Large Distal Platform Support
K233975 Zoom 6F Insert Catheters
K231168 TracStar LDP Large Distal Platform; Zoom 88 Large Distal Platform; Zoom 88 Large Distal Platform Support
K220807 Imperative Care Radial 088 Access System
K212224 TracStar LDP Large Distal Platform; Zoom 88 Large Distal Platform
Search all 17 clearances from Imperative Care, Inc. →