# K071246: Micrus Microcoil Delivery System, Models SPH, Hel, Che, PC4, HSR, FSR, CSP, CFS, SRC, PP4, STR

- Pathway: 510(k) (Special)
- Applicant: Micrus Endovascular Corporation
- Decided: Jun 1, 2007 after 29 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: 7 generations back to K951256 (1995). 27 ancestors in all.
No later device cites it as a predicate yet.
0 of 28 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K002056: Micrus Microcoil Delivery System, MDS03, Micrus Corp. (2001) Summary page 1.
- K031578: Micrus Microcoil Systems, Models Hel, SPH, STR, FSR and HSR, Micrus Corp. (2003) Summary page 1.

## Indications for use
The Micrus Microcoil Delivery System is intended for endovascular embolization of intracranial aneurysms.

Source page: https://510kreport.com/device/K071246
Methodology: https://510kreport.com/methodology