# K072379: MPS Oxiport and MPS Oxiport Plus

- Pathway: 510(k) (Special)
- Applicant: Innerspace, Inc.
- Decided: Apr 29, 2008 after 249 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 K002765 (2000). 12 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K041838: MPS (or MPS-T), Innerspace, Inc. (2005) Summary page 1.
- K962928: Combined Intracranial Pressure-Temperature Sensing System (Icp/), Camino Neurocare, Inc. (1996) Summary page 1.
- K003905: Acti-Icp Monitoring System, Innerspace, Inc. (2001) Summary page 1.
- (no number) Camino: named in the summary without a submission number
- (no number) Codman: named in the summary without a submission number

## Most influential descendants
- K083378: Synergy (2009), 1 descendant of its own
- K161010: HICP200 Patient/Monitor Interconnect Cable (2016), 0 descendants of its own

## Indications for use
The use of a Hummingbird HUMV-500 or HUMV-500MR by a qualified neurosurgeon is indicated when direct measurement of intracranial pressure is clinically important, when the patient may require CSF drainage in the course of their care, when data from one or more parameters may be deemed useful in providing optimum patient management and, in the case of the Hummingbird-500MR, when an MRI may be indicated.

Source page: https://510kreport.com/device/K072379
Methodology: https://510kreport.com/methodology