# K960715: Pruitt-Inahara Carotid Shunt 400-40-8F/Inahara-Pruitt Carotid Shunt 500-50-8F

- Pathway: 510(k) (Traditional)
- Applicant: Ideas For Medicine, Inc.
- Decided: Sep 9, 1996 after 201 days
- Product code: MJN (Catheter, Intravascular Occluding, Temporary)
- Device class: 2
- Regulation: 21 CFR 870.4450
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 1 cites it directly.
0 of 8 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) 9 French Pruitt-Inahara Shunts: named in the summary without a submission number

## Most influential descendants
- K043023: Pruitt-Inahara Outlying Carotid Shunt, Models, 2012-49, 2013-49, 2014-49,2015-49,2016-49, 2017-49 (2004), 6 descendants of its own
- K051067: Pruitt F3 Outlying and Inlying Carotid Shunt (with and Without T-Port) (2005), 5 descendants of its own
- K143454: Pruitt F3-S Carotid Shunt (2015), 1 descendant of its own
- K182916: Pruitt F3 Carotid Shunt, 10 Fr, Pruitt F3 Carotid Shunt, 9 Fr, Pruitt F3 Carotid Shunt, 8 Fr (2018), 0 descendants of its own
- K152833: Pruitt F3-S Polyurethane Carotid Shunt (2016), 0 descendants of its own

## Indications for use
The intended use of these devices is to provide a temporary bypass during carotid endarterectomy.

Source page: https://510kreport.com/device/K960715
Methodology: https://510kreport.com/methodology