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- MiscellaneousMiscellaneous
- Subpart B—Cardiovascular Diagnostic DevicesCFR Sub-Part
- MOFGuide, Wire, Catheter, Neurovasculature2Product Code
- NDQSystem, Catheter Or Guidewire, Steerable (Magnetic)2Product Code
- NRYCatheter, Thrombus Retriever2Product Code
- NUIUltrasound, Infusion, System2Product Code
- QBECranial Sound Monitor2Product Code
- QJPCatheter, Percutaneous, Neurovasculature2Product Code
- K241768Broadway 8 Catheter (BRW084132-01)2Cleared 510(K)
- K241637Echo Intracranial Base Catheter2Cleared 510(K)
- K242033Access25™ Delivery Microcatheter2Cleared 510(K)
- K24097187 NeuGlide Catheter2Cleared 510(K)
- K242301Socrates 38 Catheter2Cleared 510(K)
- K240746Neurovascular Access System Family2Cleared 510(K)
- K240711Zipline Access Catheter2Cleared 510(K)
- K241244CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter2Cleared 510(K)
- K2405298F Modified Sheath System2Cleared 510(K)
- K234074Next Generation Access Catheter2Cleared 510(K)
Show All 66 Submissions
- Subpart B—Diagnostic DevicesCFR Sub-Part
- Subpart B—Neurological Diagnostic DevicesCFR Sub-Part
- Subpart B—Physical Medicine Diagnostic DevicesCFR Sub-Part
- Subpart C—Cardiovascular Monitoring DevicesCFR Sub-Part
- Subpart D—Physical Medicine Prosthetic DevicesCFR Sub-Part
- Subpart E—Neurological Surgical DevicesCFR Sub-Part
- Subpart E—Surgical DevicesCFR Sub-Part
- Subpart F—Cardiovascular Therapeutic DevicesCFR Sub-Part
- Subpart F—Neurological Therapeutic DevicesCFR Sub-Part
- Subpart F—Physical Medicine Therapeutic DevicesCFR Sub-Part
- Subpart F—Therapeutic DevicesCFR Sub-Part
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Echo Intracranial Base Catheter
- Page Type
- Cleared 510(K)
- FDA Hosted PDF* The FDA doesn't provide PDFs for all submissions.
- 510(k) Number
- K241637
- 510(k) Type
- Traditional
- Applicant
- Stryker Neurovascular
- Country
- United States
- FDA Decision
- Substantially Equivalent
- Decision Date
- 12/19/2024
- Days to Decision
- 195 days
- Submission Type
- Summary