Kyphoplasty systems
Spider Kolibri
A device intended to be used to dilate a body lumen or access channel to facilitate the introduction of endoscopic instruments percutaneously (through the skin) or through a natural orifice (e.g., urethra). It may be a flexible or rigid rod/tube with a tapered distal tip. This is a single-use device.
Where to buy Spider Kolibri
We do not have contact details for Sintea Plustek Srl yet. Send a request and we will route it to the right person for your country.
Spider Kolibri 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 |
|---|---|---|---|
| SPS-26S540 | — | MR Unsafe | Available |
| SPS-26S545 | — | MR Unsafe | Available |
| SPS-26S550 | — | MR Unsafe | Available |
| SPS-26S640 | — | MR Unsafe | Available |
| SPS-26S645 | — | MR Unsafe | Available |
| SPS-26S650 | — | MR Unsafe | Available |
| SPS-27S540 | — | MR Unsafe | Available |
| SPS-27S545 | — | MR Unsafe | Available |
| SPS-27S550 | — | MR Unsafe | Available |
| SPS-27S640 | — | MR Unsafe | Available |
| SPS-27S645 | — | MR Unsafe | Available |
| SPS-27S650 | — | MR Unsafe | Available |
FDA clearances
- 510(k) K130402 April 2013
Procedures that use kyphoplasty systems
Frequently asked questions
What is Spider Kolibri used for?
A device intended to be used to dilate a body lumen or access channel to facilitate the introduction of endoscopic instruments percutaneously (through the skin) or through a natural orifice (e.g., urethra). It may be a flexible or rigid rod/tube with a tapered distal tip. This is a single-use device.
Who makes Spider Kolibri?
Spider Kolibri is made by Sintea Plustek Srl. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does Spider Kolibri come in?
The FDA device database does not list sizes for Spider Kolibri. Check the instructions for use or ask a Sintea Plustek Srl representative.
Is Spider Kolibri MRI safe?
The FDA device database lists Spider Kolibri as MR Unsafe. Always follow the specific MRI conditions in the labeling.
Is Spider Kolibri FDA cleared?
Spider Kolibri is covered by FDA submission K130402.
How do I contact a Sintea Plustek Srl sales representative?
Sintea Plustek Srl has not listed representatives on LA Vascular yet. Visit the Sintea Plustek Srl 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.