Onyx® HD-500
Expanded Options
Onyx® is a non-adhesive liquid embolic agent used for the embolization of brain aneurysms.
- Onyx HD500 is comprised of 20% EVOH (ethylene vinyl alcohol) copolymer dissolved in DMSO (dimethyl sulfoxide), and suspended micronized tantalum powder to provide contrast for visualization under fluoroscopy.
- Onyx HD500 (20% EVOH) is an HDE device for the treatment of intracranial, saccular, sidewall aneurysms that present with a wide neck (≥ 4mm) or with a dome-to-neck ratio < 2 that are not amenable to treatment with surgical clipping.
- Onyx HD500 can also be used in adjunctive therapy with Axium coils and stents.
| Onyx® HD-500 Liquid Embolic System | |||
| Product Name | Product Catalog Number | ||
|---|---|---|---|
| Onyx HD-500 | 105-8101-500 | ||
For the treatment of intracranial, saccular, sidewall aneurysms that present with a wide neck (≥ 4mm) or with a dome-to-neck ratio < 2 that are not amenable to treatment with surgical clipping.
Indications, contraindications, warnings and instructions for use can be found in the product labeling supplied with each device. CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician.
Humanitarian Device. Authorized by federal law for use in the intracranial, saccular, sidewall aneurysms that present with a wide neck (>4 mm) or with a dome-to-neck ratio < 2 that are not amenable to treatment with surgical clipping. The effectiveness of this device for this use has not been demonstrated.
CONTRAINDICATIONS: The use of Onyx LES is contraindicated when any of the following conditions exist: 1. When optimal catheter placement is not possible; 2. When provocative testing indicates intolerance to the occlusion procedure; AND 3: When vasospasm stops blood flow. Onyx Liquid Embolic System for Onyx HD-500 Essential Product Information (EPI).
Humanitarian Device. Authorized by federal law for use in the intracranial, saccular, sidewall aneurysms that present with a wide neck (>4 mm) or with a dome-to-neck ratio < 2 that are not amenable to treatment with surgical clipping. The effectiveness of this device for this use has not been demonstrated.
CONTRAINDICATIONS: The use of Onyx LES is contraindicated when any of the following conditions exist: 1. When optimal catheter placement is not possible; 2. When provocative testing indicates intolerance to the occlusion procedure; AND 3: When vasospasm stops blood flow. Onyx Liquid Embolic System for Onyx HD-500 Essential Product Information (EPI).



