# K133754: Integra Camino Flex Ventricular Intracranial Pressure Monitoring Kit with Flex Adapter

- Pathway: 510(k) (Traditional)
- Applicant: Integra LifeSciences Corporation
- Decided: Mar 6, 2014 after 87 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: 3 generations back to K813459 (1982). 9 ancestors in all.
No later device cites it as a predicate yet.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K121159: Integra Camino Flex Ventricular Intracranial Pressure Monitoring Kit with Intrgra Camino Flex Adapter, Integra Lifescience Corportation (2012) Summary page 1.

## Indications for use
Use of the lntegrTM Camino® Flex Ventricular Intracranial Pressure Monitoring Kit is indicated when direct and Continuous intraventricular intracranial pressure (ICP) monitoring and cerebrospinal fluid (CSF) drainage are required.

Source page: https://510kreport.com/device/K133754
Methodology: https://510kreport.com/methodology