# K063653: Micrus Microcoil System, Cashmere Model SRC

- Pathway: 510(k) (Special)
- Applicant: Micrus Endovascular Corporation
- Decided: Jan 17, 2007 after 40 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: 6 generations back to K951256 (1995). 31 ancestors in all.
35 later devices descend from it; 2 cite it directly.
1 of 67 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K022420: Micrus Stretch-Resistant Microcoil System, MSR01, Micrus Corp. (2002) Summary page 1.
- K002056: Micrus Microcoil Delivery System, MDS03, Micrus Corp. (2001) Summary page 1.
- K042539: GDC-10 360 Degree Coil SR; GDC-10 360 Degree Soft Coil SR; GDC-18 360 Degree Coil, Boston Scientific Corp (2004) Summary page 1.
- K032553: Trufill DCS Orbit Detachable Coil and Trufill DCS Syringe, Also Known as Trufill DCS Orbit Detachable Coil System, Cordis Neurovascular, Inc. (2003) Summary page 1.

## Most influential descendants
- K070707: Micrus Microcoil System (2007), 32 descendants of its own
- K073442: Micrus Microcoil Systems (2008), 31 descendants of its own
- K081465: Axium Detachable Coil System (2008), 22 descendants of its own
- K123803: Reverse Medical Micro Vascular Plug (MVP) System (2013), 10 descendants of its own
- K072173: Micrus Microcoil System Cashmere-Cerecyte, Model CRC; Cashmere-SR, Model SRC (2007), 9 descendants of its own

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

Source page: https://510kreport.com/device/K063653
Methodology: https://510kreport.com/methodology