Data / Medical devices / United States / Crossroads Neurovascular
Crossroads Neurovascular: FDA-registered device maker in Lake Forest, CA, United States, 1 510(k) clearance
Crossroads Neurovascular is registered with the FDA (registration 3032047719) in Lake Forest, CA, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 9, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3032047719
- Address
- 105 North Pointe Drive Suite D, Lake Forest, CA, United States, 92630
- Owner or operator
- Crossroads Neurovascular (10091269)
- Roles
- Manufacturer for export, Specification developer
- First device listed
- August 6, 2024
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter, Percutaneous | DQY | 2 | Manufacturer for export | accessdata.fda.gov |
| Catheter, Percutaneous, Neurovasculature | QJP | 2 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 9, 2025 | K242392 | PATH BGC | QJP | Substantially Equivalent | Crossroads Neurovascular, Inc. | accessdata.fda.gov |
Compare with other makers
Updated May 9, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.