# K102101: Surgivision MR Compatible Ventricular Cannula

- Pathway: 510(k) (Traditional)
- Applicant: Surgivision, Inc.
- Decided: Jan 26, 2011 after 183 days
- Product code: HCD (Cannula, Ventricular)
- Device class: 1
- Regulation: 21 CFR 882.4060
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 3 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Adson Cannula: named in the summary without a submission number

## Most influential descendants
- K150660: Alcyone MEMS Cannula (AMC) System (2015), 1 descendant of its own
- K123605: Smartflow Catheter (2013), 1 descendant of its own
- K161731: Cleveland Multiport Ventricular Catheter Set (2017), 0 descendants of its own

## Indications for use
The MR Compatible Ventricular Cannula is intended for injection of Cytarabine or removal of CSF from the ventricles during intracranial procedures. The device is not intended for implant. The device is intended for "single patient use only."

Source page: https://510kreport.com/device/K102101
Methodology: https://510kreport.com/methodology