Coils
Cerecyte Presidio
A non-bioabsorbable, implantable device intended to induce a neurovascular thrombosis to treat an intracranial aneurysm and/or neurovascular arteriovenous malformation (AVM); it may also be intended to treat non-neurovascular malformations. It is in the form of a metal [e.g., platinum alloy] or metal/synthetic polymer wire which coils upon deployment within the aneurysm/vasculature; it is typically pre-attached to a nonimplantable delivery wire. Disposable devices associated with implantation (e.g., delivery wire, catheter) may be included.
Cerecyte Presidio models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| PC4100412-30 | Length 11.5 cm; Length 190 cm | MR Conditional | Available |
| PC4100517-30 | Length 17 cm; Length 190 cm | MR Conditional | Available |
| PC4100626-30 | Length 26 cm; Length 190 cm | MR Conditional | Available |
| PC4100730-30 | Length 30 cm; Length 190 cm | MR Conditional | Available |
| PC4100829-30 | Length 29 cm; Length 190 cm | MR Conditional | Available |
| PC4180830-30 | Length 30 cm; Length 190 cm | MR Conditional | Available |
| PC4180933-30 | Length 33 cm; Length 190 cm | MR Conditional | Available |
| PC4181034-30 | Length 34 cm; Length 190 cm | MR Conditional | Available |
| PC4181137-30 | Length 37 cm; Length 190 cm | MR Conditional | Available |
| PC4181240-30 | Length 40 cm; Length 190 cm | MR Conditional | Available |
| PC4181343-30 | Length 43 cm; Length 190 cm | MR Conditional | Available |
| PC4181447-30 | Length 47 cm; Length 190 cm | MR Conditional | Available |
| PC4181550-30 | Length 50 cm; Length 190 cm | MR Conditional | Available |
| PC4181647-30 | Length 47 cm; Length 190 cm | MR Conditional | Available |
| PC4181750-30 | Length 50 cm; Length 190 cm | MR Conditional | Available |
| PC4181846-30 | Length 46 cm; Length 190 cm | MR Conditional | Available |
| PC4181950-30 | Length 50 cm; Length 190 cm | MR Conditional | Available |
| PC4182050-30 | Length 50 cm; Length 190 cm | MR Conditional | Available |
FDA clearances
- 510(k) K082739 October 2008
- 510(k) K032872 November 2003
Procedures that use coils
Frequently asked questions
What is Cerecyte Presidio used for?
A non-bioabsorbable, implantable device intended to induce a neurovascular thrombosis to treat an intracranial aneurysm and/or neurovascular arteriovenous malformation (AVM); it may also be intended to treat non-neurovascular malformations. It is in the form of a metal [e.g., platinum alloy] or metal/synthetic polymer wire which coils upon deployment within the aneurysm/vasculature; it is typically pre-attached to a nonimplantable delivery wire. Disposable devices associated with implantation (e.g., delivery wire, catheter) may be included.
Who makes Cerecyte Presidio?
Cerecyte Presidio is made by Medos International Sàrl. It is listed under embolization coils in our device library.
What sizes does Cerecyte Presidio come in?
Sizes listed for Cerecyte Presidio: Length: 11.5–190 cm. Confirm availability with the manufacturer's instructions for use.
Is Cerecyte Presidio MRI safe?
The FDA device database lists Cerecyte Presidio as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Cerecyte Presidio FDA cleared?
Cerecyte Presidio is covered by FDA submissions K082739, K032872.
How do I contact a Medos International Sàrl sales representative?
Medos International Sàrl has not listed representatives on LA Vascular yet. Visit the Medos International Sàrl company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.