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

Penumbra System (Thunderbolt Aspiration Tubing)

K Number: K250690 · Decision Jun 10, 2026
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
108
Applicant Total
87
Review Days
460

Basic Information

Device Name
Penumbra System (Thunderbolt Aspiration Tubing)
K Number
K250690
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Penumbra, Inc.
Date Received
March 7, 2025
Decision Date
June 10, 2026
Product Code
NRY
Advisory Committee
Cardiovascular
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NRY Catheter, Thrombus Retriever

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Other Clearances by Penumbra, Inc.

K Number Device Name
K260599 INDIGO® Aspiration System – INDIGO Link
K251949 INDIGO® Aspiration System - Lightning Flash Aspiration Tubing with LINK
K252612 INDIGO® Aspiration System – Lightning Flash Aspiration Tubing; INDIGO® Aspiration System – Lightning Bolt Aspiration Tubing
K250079 Ruby XL System
K242104 Penumbra System (Reperfusion Catheter RED 72)
K242033 Access25™ Delivery Microcatheter
K242520 Element Vascular Access System
K242075 Indigo® Aspiration System – Lightning Bolt Aspiration Tubing
K242319 Indigo® Aspiration System – Aspiration Catheter 6X
K241399 Indigo® Lightning Flash Aspiration System – Select +™ Catheter
Search all 87 clearances from Penumbra, Inc. →