Vascular plugs
Harbor
A non-bioabsorbable, metal device intended to be implanted in a non-neurovascular blood vessel, permanently or long-term, to occlude blood flow typically for treatment of an aneurysm, tumour (e.g., nephroma, hepatoma, uterine fibroids), and/or arteriovenous malformation (AVM). It is in the form of an expandable metal scaffold, which once expanded is intended to induce thrombosis and create a blockage; it is typically supplied with instruments dedicated to implantation. This device is not intended to be used in intracranial arteries or for other neurovascular applications.
Harbor 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 |
|---|---|---|---|
| 04-OCCLUDE-020 | — | MR Conditional | Available |
| 04-OCCLUDE-025 | — | MR Conditional | Available |
| 04-OCCLUDE-030 | — | MR Conditional | Available |
| 04-OCCLUDE-035 | — | MR Conditional | Available |
| 04-OCCLUDE-040 | — | MR Conditional | Available |
| 04-OCCLUDE-045 | — | MR Conditional | Available |
| 04-OCCLUDE-050 | — | MR Conditional | Available |
| 04-OCCLUDE-055 | — | MR Conditional | Available |
| 04-OCCLUDE-060 | — | MR Conditional | Available |
| 04-OCCLUDE-065 | — | MR Conditional | Available |
| 04-OCCLUDE-070 | — | MR Conditional | Available |
| 04-OCCLUDE-080 | — | MR Conditional | Available |
| 04-OCCLUDE-090 | — | MR Conditional | Available |
| 04-OCCLUDE-100 | — | MR Conditional | Available |
| 04-OCCLUDE-110 | — | MR Conditional | Available |
| 04-OCCLUDE-120 | — | MR Conditional | Available |
FDA clearances
- 510(k) K250133 July 2025
Procedures that use vascular plugs
Frequently asked questions
What is Harbor used for?
A non-bioabsorbable, metal device intended to be implanted in a non-neurovascular blood vessel, permanently or long-term, to occlude blood flow typically for treatment of an aneurysm, tumour (e.g., nephroma, hepatoma, uterine fibroids), and/or arteriovenous malformation (AVM). It is in the form of an expandable metal scaffold, which once expanded is intended to induce thrombosis and create a blockage; it is typically supplied with instruments dedicated to implantation. This device is not intended to be used in intracranial arteries or for other neurovascular applications.
Who makes Harbor?
Harbor is made by Nuvascular, Inc.. It is listed under vascular plugs (amplatzer and micro vascular plugs) in our device library.
What sizes does Harbor come in?
The FDA device database does not list sizes for Harbor. Check the instructions for use or ask a Nuvascular, Inc. representative.
Is Harbor MRI safe?
The FDA device database lists Harbor as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Harbor FDA cleared?
Harbor is covered by FDA submission K250133.
How do I contact a Nuvascular, Inc. sales representative?
Nuvascular, Inc. has not listed representatives on LA Vascular yet. Visit the Nuvascular, Inc. 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.