510(k) Report

510(k) · Cleared

Cleared

Micrus Microcoil System, Cashmere Model SRC

K063653510(k) SpecialCleared Jan 17, 200740-day reviewClass II21 CFR 882.5950

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Micrus Endovascular Corporation · HCG Device, Neurovascular Embolization

Cleared on Jan 17, 2007 as substantially equivalent to K022420 (Micrus Corp., 2002) and 3 other predicates after a 40-day review. Its family tree reaches back 6 generations to 1995. 1 of the 67 devices in its family, counting itself, has a Class I recall. 35 later devices descend from it.

Decided
Jan 17, 2007
Review
40 days
Class
Class II
Product code
HCG
Recalls
None
Predicates
4

Its longest line of descent runs back 6 generations to K951256 (1995). 31 ancestors in all, the oldest K860840 (1986). 35 later devices descend from it, 2 citing it directly. 1 of the 67 devices in this family, counting this one, has a Class I recall.

Other ancestors, by year clearedDescendants, by year cleared 2004: 1 other ancestor2003: 2 other ancestors2001: 1 other ancestor2000: 1 other ancestor1999: 1 other ancestor1994: 2 other ancestors1992: 5 other ancestors1997: 1 other ancestor1996: 2 other ancestors1995: 2 other ancestors1991: 2 other ancestors1989: 1 other ancestor1988: 3 other ancestors1986: 1 other ancestor2007: 2 descendants cleared2008: 3 descendants cleared2014: 4 descendants cleared2012: 1 descendant cleared2015: 4 descendants cleared2013: 2 descendants cleared2017: 3 descendants cleared2009: 1 descendant cleared2021: 3 descendants cleared2022: 3 descendants cleared, 1 with a Class I recall12018: 3 descendants cleared2026: 3 descendants cleared2020: 1 descendant cleared2023: 1 descendant cleared2019: 1 descendant clearedK951256 · Detachable Platinum Coil (Guglielmi Detachable Coil, GDC) · Target Therapeutics · 1995×2: 2 generations cleared close together, K960705 (1996), K962503 (1996) K971395 · Guglielmi Detachable Coil (GDC), Fibered Platinum Coil, .035 Type, Berenstein Liquid Coil, Fibered Platinum Coils, Acce · Target Therapeutics · 1997K993415 · GDC-10 Stretch Resistant Guglielmi Detachable Coil, GDC-10 2-Diameter Stretch Resistant Guglielmi Detachable Coil, GDC-1 · Boston Scientific, Target · 2000K022420 · Micrus Stretch-Resistant Microcoil System, MSR01 · Micrus Corp. · 20021990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 3 other ancestors2 generations back: 3 other ancestors3 generations back: 2 other ancestors4 generations back: 16 other ancestors5 generations back: 1 other ancestor 1 generation forward: 2 descendants2 generations forward: 4 descendants3 generations forward: 2 descendants4 generations forward: 9 descendants, 1 with a Class I recall15 generations forward: 9 descendants6 generations forward: 6 descendants7 generations forward: 3 descendants K022420 · Micrus Stretch-Resistant Microcoil System, MSR01 · Micrus Corp. · 2002K993415 · GDC-10 Stretch Resistant Guglielmi Detachable Coil, GDC-10 2-Diameter Stretch Resistant Guglielmi Detachable Coil, GDC-1 · Boston Scientific, Target · 2000K971395 · Guglielmi Detachable Coil (GDC), Fibered Platinum Coil, .035 Type, Berenstein Liquid Coil, Fibered Platinum Coils, Acce · Target Therapeutics · 1997K962503 · Guglielmi Detachable Coil · Target Therapeutics · 1996K960705 · Guglielmi Detachable Coil · Target Therapeutics · 1996K951256 · Detachable Platinum Coil (Guglielmi Detachable Coil, GDC) · Target Therapeutics · 1995−50+5
  1. Root · 6 generations backK951256 Detachable Platinum Coil (Guglielmi Detachable Coil, GDC)Target Therapeutics · 1995
  2. 5 generations backK960705 Guglielmi Detachable CoilTarget Therapeutics · 1996
  3. 4 generations backK962503 Guglielmi Detachable CoilTarget Therapeutics · 1996
  4. 3 generations backK971395 Guglielmi Detachable Coil (GDC), Fibered Platinum Coil, .035 Type…Target Therapeutics · 1997
  5. 2 generations backK993415 GDC-10 Stretch Resistant Guglielmi Detachable Coil, GDC-10…Boston Scientific, Target · 2000
  6. 1 generation backK022420 Micrus Stretch-Resistant Microcoil System, MSR01Micrus Corp. · 2002
  7. This deviceK063653 Micrus Microcoil System, Cashmere Model SRCMicrus Endovascular Corporation · 2007
  8. Descendant · cites it directly · 32 of its ownK070707 Micrus Microcoil SystemMicrus Endovascular Corporation · 2007
  9. Descendant · 2 generations on · 31 of its ownK073442 Micrus Microcoil SystemsMicrus Endovascular Corporation · 2008
  10. Descendant · 3 generations on · 22 of its ownK081465 Axium Detachable Coil SystemMicro Therapeutics, Inc. · 2008 · Recalled
  11. Descendant · 4 generations on · 10 of its ownK123803 Reverse Medical Micro Vascular Plug (MVP) SystemReverse Medical Corporation · 2013
  12. Descendant · cites it directly · 9 of its ownK072173 Micrus Microcoil System Cashmere-Cerecyte, Model CRC; Cashmere-SR…Micrus Endovascular Corporation · 2007 · Recalled

Showing 5 of 35 descendants. See all descendants

Descendants cleared per year

2007: 22008: 32009: 12012: 12013: 22014: 42015: 42017: 32018: 32019: 12020: 12021: 32022: 32023: 12026: 3
2007high 4 (2014) · low 0 (2010)2026

Class I recalls in this family

Most influential descendants

Showing 5 of 35 · See all
  • K070707Micrus Microcoil SystemMicrus Endovascular Corporation · 2007 · cites it directly32descendants
  • K073442Micrus Microcoil SystemsMicrus Endovascular Corporation · 2008 · 2 generations on31descendants
  • K081465Axium Detachable Coil SystemMicro Therapeutics, Inc. · 2008 · 3 generations on22descendants
  • K123803Reverse Medical Micro Vascular Plug (MVP) SystemReverse Medical Corporation · 2013 · 4 generations on10descendants
  • K072173Micrus Microcoil System Cashmere-Cerecyte, Model CRC; Cashmere-SR, Model SRCMicrus Endovascular Corporation · 2007 · cites it directly9descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K951256Detachable Platinum Coil (Guglielmi Detachable Coil, GDC)Target Therapeutics1995—
−5K960705Guglielmi Detachable CoilTarget Therapeutics1996—
−4K962503Guglielmi Detachable CoilTarget Therapeutics1996—
−3K971395Guglielmi Detachable Coil (GDC), Fibered Platinum Coil, .035 Type, Berenstein…Target Therapeutics1997—
−2K993415GDC-10 Stretch Resistant Guglielmi Detachable Coil, GDC-10 2-Diameter Stretch…Boston Scientific, Target2000—
−1K022420Micrus Stretch-Resistant Microcoil System, MSR01Micrus Corp.2002—
0 (this device)K063653Micrus Microcoil System, Cashmere Model SRCMicrus Endovascular Corporation2007—
+1K070707Micrus Microcoil SystemMicrus Endovascular Corporation2007—
+2K073442Micrus Microcoil SystemsMicrus Endovascular Corporation2008—
+3K081465Axium Detachable Coil SystemMicro Therapeutics, Inc.20082
+4K123803Reverse Medical Micro Vascular Plug (MVP) SystemReverse Medical Corporation2013—
+1K072173Micrus Microcoil System Cashmere-Cerecyte, Model CRC; Cashmere-SR, Model SRCMicrus Endovascular Corporation20071

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198610
198830
198910
199120
199250
199420
199520
199620
199710
199910
200010
200110
200320
200410

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200720
200830
200910
201210
201320
201440
201540
201730
201830
201910
202010
202130
202231
202310
202630
FIG. 1 — Lineage of K063653, 1995–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

1 device in this family has a Class I recall. A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new HCG device

  1. #1 K252700 Optima Coil System (Optima Packing Coil System)score 20.6 · 26 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (4)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K022420Micrus Stretch-Resistant Microcoil System, MSR01
Summary page 1
…ification Name: Device, Artificial Embolization Regulatory Class II Predicate Devices: Micros Stretch-Resistant Microcoil, 510(k) no.K022420 Micrus Microcoil Delivery System, 510(k) no. K002056 Boston Scientific GDC…
Micrus Corp.2002—
*K002056Micrus Microcoil Delivery System, MDS03
Summary page 1
…latory Class II Predicate Devices: Micros Stretch-Resistant Microcoil, 510(k) no.K022420 Micrus Microcoil Delivery System, 510(k) no. K002056 Boston Scientific GDC 360 Soft SR, 510(k) no. K042539 Cordis Trufill DCS Or…
Micrus Corp.2001—
*K042539GDC-10 360 Degree Coil SR; GDC-10 360 Degree Soft Coil SR; GDC-18 360 Degree Coil
Summary page 1
…10(k) no.K022420 Micrus Microcoil Delivery System, 510(k) no. K002056 Boston Scientific GDC 360 Soft SR, 510(k) no. K042539 Cordis Trufill DCS Orbit Detachable Coil, 5 10(k) no.K032553 Device Description: The Micrus Ca…
Boston Scientific Corp20042
*K032553Trufill DCS Orbit Detachable Coil and Trufill DCS Syringe, Also Known as Trufill DCS…
Summary page 1
…K002056 Boston Scientific GDC 360 Soft SR, 510(k) no. K042539 Cordis Trufill DCS Orbit Detachable Coil, 5 10(k) no.K032553 Device Description: The Micrus Cashmere-14 MicroCoil System consists of an embolic coil ("Micr…
Cordis Neurovascular, Inc.2003—

Also cleared against K022420: 3 other devices →

What descends from it? (35)

See all 35

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K070707Micrus Microcoil SystemMicrus Endovascular Corporation200732
K072173Micrus Microcoil System Cashmere-Cerecyte, Model CRC; Cashmere-SR, Model SRCMicrus Endovascular Corporation20079

Has anything in its family been recalled? (1 Class I)

No FDA recall names this device.

Relatives with a Class I recall

Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.

  • K220040CEREPAK Uniform, Uniform XL, Uniform 3D, Heliform Soft, Heliform XtraSoft, Heliform XL, Heliform XtraSoft…Medos International SARL · 2022 · 4 generations on · ◆ in the 2022 descendants bar of FIG. 11 Class I recall

What does this lineage say?

  • The line of descent spans 12 years and passes through 4 companies; a new generation was cleared every 2.5 years on median.
  • 4 of the 31 ancestors have a recall of any class.
  • Of its descendants, K070707 (Micrus Endovascular Corporation, 2007) has gone furthest, with 32 descendants of its own.
  • 3 other devices also cite its predicate K022420.

How does its category compare?

All HCG devices

HCG Device, Neurovascular Embolization: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.

FDA decisions per year · HCG

3in 2025

2007: 82008: 92009: 72010: 82011: 92012: 72013: 72014: 52015: 52016: 72017: 52018: 42019: 12020: 22021: 52022: 32023: 22024: 42025: 32026 (partial year): 4
2007high 9 (2008) · low 1 (2019)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HCG

107in 2025

2007: 50 days median2008: 71 days median2009: 48 days median2010: 72 days median2011: 78 days median2012: 30 days median2013: 67 days median2014: 66 days median2015: 60 days median2016: 37 days median2017: 97 days median2018: 173 days median2021: 103 days median2022: 114 days median2024: 49 days median2025: 107 days median2026 (partial year): 30 days median
2007high 173 (2018) · low 30 (2012)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · HCG

1in 2025

2007: 12008: 32010: 22011: 12013: 22014: 42022: 22024: 12025: 1, 1 Class I2026 (partial year): 1
2007high 4 (2014) · low 0 (2009)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · HCG

537in 2025

2007: 3262008: 7302009: 8212010: 8512011: 8942012: 1,1462013: 1,1032014: 1,7292015: 1,5982016: 1,9912017: 2,4942018: 2,0582019: 1,7632020: 1,7542021: 2,2682022: 6632023: 5682024: 5522025: 537
2007high 2,494 (2017) · low 326 (2007)2025

MAUDE reports naming product code HCG, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20078501326
20089713730
20097480821
20108722851
20119781894
201273001,146
201376721,103
201456641,729
201556001,598
201673701,991
201759702,494
2018417302,058
20191—01,763
20202—01,754
2021510302,268
202231142663
20232—0568
20244491552
202531071 (1)537
20264301—

What is it indicated for?

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

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K063653: Micrus Microcoil System, Cashmere Model SRC.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K063653

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026