CROSSROADS NEUROVASCULAR

FDA Device Registration & Listing · Lake Forest, CA, US · Registration 3032047719

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3032047719
FEI Number
3032047719
Entity Name
CROSSROADS NEUROVASCULAR
City/State/Country
Lake Forest, CA, US
Establishment Address
105 North Pointe Drive, Suite D, Lake Forest, CA 92630, US
Establishment Type(s)
Manufacture Device in the United States for Export Only
Owner / Operator
Crossroads Neurovascular (Owner Number: 10091269)
Owner / Operator Contact Address
105 North Pointe Drive, Suite D, Lake Forest, CA 92630, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DQY Catheter, Percutaneous Cardiovascular Class 2 870.1250 2024-08-06

Official Correspondent

Ryan Breckenridge

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Crossroads Neurovascular
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K043580 Chestnut Medical Technologies, Inc. ALLIGATOR RETRIEVAL DEVICE (ARD) 2005-03-24
K982883 Medtronics Interventional Vascular MEDTRONIC 7F AND 8F ZUMA GUIDING CATHETER 1998-09-04
K132420 Reflow Medical WINGMAN EXTENDABLE TIP SUPPORT CATHETER 2013-09-19
K082339 Endocross, Ltd. ENABLER-P SUPPORT CATHETER 2008-11-20
K210009 CenterPoint Systems, LLC Guiding Catheter 2021-11-24

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0001-2010 Penumbra Inc. 2
Penumbra Neuron Delivery Catheter 070, percutaneous catheter, catalog numbers PND6F0701058, PND6F070956, PND6F0701058M, and PND6F070956M; manufactured by Penumbra, Inc., Alameda, CA. Indicated for the introduction of interventional devices into the peripheral, coronary, and neuro vasculature.
Z-0003-2014 Cordis Corporation 2
Cordis ADROIT 6F Guiding Catheter Product Usage: For intravascular introduction of interventional and/or diagnostic devices into the coronary or peripheral vascular system.
Z-0009-2024 Boston Scientific Corporation 2
Guider Softip Guide Catheter 6F PRE-SHAPED 40 90CM, Catalog number H965100420, cardiac guide catheter
Z-0010-04 Bard Peripheral Vascular 2
Conquest Balloon Dilation Catheters Model/Catalog Number CQ 75124
Z-0010-2024 Boston Scientific Corporation 2
Guider Softip Guide Catheter 7F PRE-SHAPED 40 90CM, Catalog number H965100430, cardiac guide catheter

Similar Registrations

Registration Number Establishment Name Location
3039062605 CORVITEX CORPORATION Raleigh, NC, US
3031768596 PIRAEUS MEDICAL, INC. Maple Grove, MN, US
3013134719 HEXACATH Rueil Malmaison Ile-de-France, FR
3011142981 Rontis Hellas S.A. Larisa Thessalia, GR
3010370269 STRAIT ACCESS TECHNOLOGIES HOLDINGS (PTY) LTD Cape Town Western Cape, ZA
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3032047719. Last updated year: 2026. Please use registration number 3032047719 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.