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

Pounce(TM) Sheath

K Number: K252227 · Decision Sep 24, 2025
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
11
Review Days
70

Basic Information

Device Name
Pounce(TM) Sheath
K Number
K252227
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Surmodics,Inc.
Date Received
July 16, 2025
Decision Date
September 24, 2025
Product Code
DYB
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
DYB Introducer, Catheter

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K Number Device Name
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K231022 Pounce™ Thrombectomy System
K221886 Sublime Microcatheter
K220501 Pounce Thrombectomy System
K211492 Pounce Thrombectomy System
K192814 Pounce Thrombus Retrieval System
K190644 Guide Sheath
K173560 Microcatheter
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