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

Pounce Thrombus Retrieval System

K Number: K192814 · Decision Sep 21, 2020
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
140
Applicant Total
11
Review Days
356

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Basic Information

Device Name
Pounce Thrombus Retrieval System
K Number
K192814
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5150
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Surmodics,Inc.
Date Received
October 1, 2019
Decision Date
September 21, 2020
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 Surmodics,Inc.

K Number Device Name
K252227 Pounce(TM) Sheath
K241362 Pounce XL Thrombectomy System (PTS-1011-7F135)
K232647 Microcatheter
K231828 Pounce™ Sheath
K231022 Pounce™ Thrombectomy System
K221886 Sublime Microcatheter
K220501 Pounce Thrombectomy System
K211492 Pounce Thrombectomy System
K190644 Guide Sheath
K173560 Microcatheter
Search all 11 clearances from Surmodics,Inc. →