# K121159: Integra Camino Flex Ventricular Intracranial Pressure Monitoring Kit with Intrgra Camino Flex Adapter

- Pathway: 510(k) (Traditional)
- Applicant: Integra Lifescience Corportation
- Decided: Jul 20, 2012 after 95 days
- Product code: GWM (Device, Monitoring, Intracranial Pressure)
- Device class: 2
- Regulation: 21 CFR 882.1620
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K813459 (1982). 8 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K904883: OPTYX, Baxter Healthcare Corp (1991) Summary page 1.
- K991222: Codman Microsensor Ventricular Catheter Kit, Johnson & Johnson Professionals, Inc. (1999) Summary page 1.
- K914735: Ventricular Pressure Monitoring Kit, Model 110-4HM, Camino Laboratories, Inc. (1992) Summary page 1.
- K962928: Combined Intracranial Pressure-Temperature Sensing System (Icp/), Camino Neurocare, Inc. (1996) Summary page 1.

## Most influential descendants
- K133754: Integra Camino Flex Ventricular Intracranial Pressure Monitoring Kit with Flex Adapter (2014), 0 descendants of its own
- K131184: Integra Licox PTO2 Monitor (2013), 0 descendants of its own

## Indications for use
The Integra Camino® Flex Ventricular Intracranial Pressure Monitoring Kit with Integra Camino® Flex Adapter is indicated when direct and continuous intraventricular intracranial pressure (ICP) monitoring and cerebrospinal fluid (CSF) drainage are required.

Source page: https://510kreport.com/device/K121159
Methodology: https://510kreport.com/methodology