Codman Libertís Shunt Catheter with Bactiseal and Endexo Technology
FDA 510(k) K243531 · Integra Lifesciences Production Corporation
510(k) numberK243531
Submission
- Device name
- Codman Libertís Shunt Catheter with Bactiseal and Endexo Technology
- Applicant
- Integra Lifesciences Production Corporation
Mansfield, MA, US - Received
- November 14, 2024
- Decision date
- August 8, 2025
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Other 510(k)s with product code JXG
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K261004 | Codman® Distal Peritoneal Catheter, Barium Open End (82-1682); Codman® HOLTER®…JXG · Traditional | Integra Lifesciences Production Corporation | 06/23/2026SE |
| K251598 | IntellidropJXG · Traditional | Brainspace, Inc. | 12/10/2025SE |
| K250636 | Sophy Mini Monopressure Valve (SM1)JXG · Traditional | Sophysa | 11/28/2025SE |
| K252514 | Evac-MriJXG · Traditional | Phasor Health, LLC | 11/05/2025SESD |
| K243552 | Codman Libertís 1.5 mm EVD Catheter with Bactiseal® and Endexo® Technology with Luer…JXG · Traditional | Integra Lifesciences Production Corporation | 08/06/2025SE |
| K242974 | External CSF Drainage Ventricular Catheters, External CSF Drainage Lumbar CathetersJXG · Traditional | Sophysa | 06/20/2025SE |
| K243205 | EvacJXG · Traditional | Phasor Health, LLC | 06/03/2025SE |
| K243676 | Duet External Drainage and Monitoring System (EDMS)JXG · Traditional | Medtronic Neurosurgery | 03/10/2025SE |
| K242003 | XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter SetJXG · Traditional | Aesculap, Inc. | 12/16/2024SE |
| K241458 | Borvo EVAC System (Ergo); Borvo EVAC System (Classic)JXG · Traditional | Borvo Medical, Inc. | 08/20/2024SE |
More from Borvo Medical, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K261004 | Codman® Distal Peritoneal Catheter, Barium Open End (82-1682); Codman® HOLTER®…JXG · Traditional | 06/23/2026SE |
| K243552 | Codman Libertís 1.5 mm EVD Catheter with Bactiseal® and Endexo® Technology with Luer…JXG · Traditional | 08/06/2025SE |
| K232890 | CereLink ICP Monitor (826820), CereLink ICP Extension Cable (826845)GWM · Traditional | 02/04/2024SE |
| K233445 | Bactiseal Catheters; Bactiseal Barium Striped Catheters; Bactiseal Endoscopic…JXG · Traditional | 01/17/2024SE |
| K233448 | Bactiseal EVD Catheter Sets; Bactiseal Clear EVD Catheter SetJXG · Traditional | 12/19/2023SE |
| K223330 | Certas Plus Programmable ValvesJXG · Traditional | 02/01/2023SE |
| K221840 | Hakim Programmable Valves, Hakim Precision Fixed Pressure ValvesJXG · Traditional | 10/14/2022SE |
| K210993 | CereLink ICP MonitorGWM · Special | 04/30/2021SE |
Questions and answers
When was Codman Libertís Shunt Catheter with Bactiseal and Endexo Technology cleared by the FDA?
Codman Libertís Shunt Catheter with Bactiseal and Endexo Technology (K243531) received a 510(k) decision of Substantially Equivalent on August 8, 2025, 267 days after the submission was received.
What is the product code of K243531?
The FDA product code is JXG – Shunt, Central Nervous System And Components, a Class II (moderate risk) device regulated under 21 CFR 882.5550.