Medical Device Manufacturer · US , Freemont , CA

Stryker Neurovascular - FDA 510(k) Cleared Devices

32 submissions · 32 cleared · Since 2011

Total

Cleared

Denied

Stryker Neurovascular, is a medical device manufacturer based in Fremont, US. The company specializes in innovative interventional neurology solutions.

Stryker Neurovascular has received 32 FDA 510(k) clearances from 32 total submissions since 2011. The company's portfolio is dominated by Neurology devices, representing 84% of regulatory submissions. The latest clearance was granted in 2026, demonstrating continued active development and market engagement.

Recent cleared devices include intracranial base catheters, detachable coils, microcatheters, and thrombectomy retrievers. These products support minimally invasive treatment of cerebrovascular conditions. The company maintains a strong focus on catheter-based interventional technologies and neurovascular access systems.

Explore the complete list of device names, product codes, and individual clearance dates in the database.

510(k) submissions have been managed by Stryker as regulatory consultant.

FDA 510(k) Regulatory Record - Stryker Neurovascular

32 devices

1-12 of 32