# K141134: Pod System

- Pathway: 510(k) (Special)
- Applicant: Penumbra, Inc.
- Decided: Jul 3, 2014 after 63 days
- Product code: HCG (Device, Neurovascular Embolization)
- Device class: 2
- Regulation: 21 CFR 882.5950
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 10 generations back to K951256 (1995). 36 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 38 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K103305: Penumbra Embolization Coil System, Penumbra, Inc. (2011) Summary page 1.
- K120330: Penumbra Coil System/Penumbra Coil 400, Penumbra, Inc. (2012) Summary page 1.

## Most influential descendants
- K170852: POD Packing Coil (2017), 0 descendants of its own

## Indications for use
The POD System is indicated for the embolization of: Intracranial aneurysms Other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae Arterial and venous embolizations in the peripheral vasculature

Source page: https://510kreport.com/device/K141134
Methodology: https://510kreport.com/methodology