Flow Diverter
Surpass Streamline - M003SFD050500
Device Description
A non-bioabsorbable tubular device typically intended to be implanted into the base or parent artery of an intracranial aneurysm (e.g., wide-neck aneurysm situated at the base of a bifurcation) to facilitate the delivery of embolics to fill the aneurysm, facilitate clotting within the aneurysm by slowing blood flow into it, and/or to provide support for a neurovascular embolization coil placed inside the aneurysm. It is made of uncoated metal [e.g., nickel-titanium alloy (Nitinol)] and self-expands after it is delivered to the site of implantation and released (e.g., from a dedicated delivery instrument). Disposable devices associated with implantation may be included.
Environmental Conditions
- Store in cool, dry, dark place.
Device Sizes
- Length: 50.0 Millimeter
- Lumen/Inner Diameter: 5.0 Millimeter
Device Sterilization
Device Sterile: True
Sterilization Prior To Use: False
Sterilization Methods: No Data Available
Product Codes
Code: OUT
Device Name: Intracranial Aneurysm Flow Diverter
Device Class: 3
Physical State: metallic
Definition: Treatment of wide-necked and larger or giant intracranial aneurysms.
Submission Type ID: 2
Review Panel: NE
Review Code: N/A
Technical Method: N
Gmp Exempt Flag: interventional
Life Sustain Support Flag: N
Unclassified Reason: N/A
Implant Flag: Y
Target Area: neurovasculature
Regulation Number: N/A
Third Party Flag: N
Medical Specialty: N/A
Device IdentifiersDevice Id: 07613252648840
Device Type: Primary
DeviceId Issuing Agency: GS1
Contains DI Number: N/A
Package Quantity: N/A
Package Discontinue Date: N/A
Package Status: N/A
Package Type: N/A