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Sign in to claim this brandSpartan Micro
US
Last updated May 23, 2026
What Spartan Micro makes
Spartan Micro manufactures manual peripheral vascular guidewires and vascular microcatheters, including the Spartan Center Wire and Spartan MC 0165 models, designed for vascular interventions.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) and UDI databases. The company is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Spartan Micro manufacture?
Spartan Micro specializes in manual peripheral vascular guidewires and vascular microcatheters. These devices are specifically designed for use in vascular interventions, such as guiding catheters or wires through blood vessels to facilitate procedures like angioplasty or stent placement. Examples include the Spartan Center Wire and Spartan MC 0165 models.
Where is Spartan Micro based?
Spartan Micro is headquartered in the United States. The company’s location is relevant for understanding its regulatory framework, as it operates under U.S. medical device regulations, including those enforced by the FDA.
Which regulatory registries list Spartan Micro’s devices?
Spartan Micro’s devices are listed in the FDA’s 510(k) premarket notification database and the Unique Device Identifier (UDI) system. These registries track devices that have undergone the required FDA review process for Class II classification, ensuring compliance with U.S. medical device regulations.
How are Spartan Micro’s devices classified under FDA regulations?
Spartan Micro’s devices, including peripheral vascular guidewires and vascular microcatheters, are classified as Class II under FDA regulations. This classification applies to devices that pose moderate risk and require special controls beyond general controls to ensure their safety and effectiveness, such as performance standards or post-market surveillance.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
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Catalogue (7)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Spartan Center Wire | FG4021 | FDA UDI | Class II | Active |
| Spartan Center Wire | FG4020 | FDA UDI | Class II | Active |
| Spartan MC 0165 | FG0006 | FDA UDI | Class II | Active |
| Spartan SC 069 | K220716 | FDA 510(k) | Class II | Active |
| Spartan eCoil System | K180653 | FDA 510(k) | Class II | Active |
| Spartan Center Wire | K220075 | FDA 510(k) | Class II | Active |
| Spartan MC 0165 | K213451 | FDA 510(k) | Class II | Active |
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