510(k) Report

510(k) · Cleared

Recalled · Class II · 2019

Microplex Coil System-Cosmos Model 100933CSSR-V, 101036CSSR-V, 101141CSSR-V, 101245CSSR-V

K093919510(k) SpecialCleared Jan 21, 201030-day reviewClass II21 CFR 882.5950Recalls 1

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

MicroVention, Inc. · HCG Device, Neurovascular Embolization

Cleared on Jan 21, 2010 as substantially equivalent to K082461 (MicroVention, Inc., 2008) and 1 other predicate after a 30-day review. Its family tree reaches back 13 generations to 1995. 8 later devices descend from it. It has been recalled once.

Decided
Jan 21, 2010
Review
30 days
Class
Class II
Product code
HCG
Recalls
1
Predicates
2

Its longest line of descent runs back 13 generations to K951256 (1995). 44 ancestors in all, the oldest K860840 (1986). 8 later devices descend from it, 3 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2003: 3 other ancestors2002: 2 other ancestors2000: 4 other ancestors1994: 3 other ancestors1992: 5 other ancestors1990: 1 other ancestor2001: 1 other ancestor1997: 1 other ancestor1996: 2 other ancestors1995: 2 other ancestors1991: 2 other ancestors1989: 1 other ancestor1988: 3 other ancestors1986: 1 other ancestor2011: 2 descendants cleared2013: 3 descendants cleared2016: 3 descendants 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 · 1997K991139 · Guglielmi Detachable (GDC) · Boston Scientific, Target · 1999K012145 · Microplex Coil System · MicroVention, Inc. · 2001K020434 · Microplex Coil System (MCS) · MicroVention, Inc. · 2002×2: 2 generations cleared close together, K032590 (2003), K033836 (2003) K041551 · Modification to: Hydrocoil Embolic System (Hes) · MicroVention, Inc. · 2004K050954 · Microplex Coil System (MCS) and Hydrocoil Embolic System (Hes) · MicroVention, Inc. · 2005 · recalledK082461 · Bare Platinum Framing Coil, Model (S) 100408BPFC-V,100412BPFC-V,100515BPFC-V100518BPFC-V,100522BPFC-V,100618BPFC-V100622B · MicroVention, Inc. · 2008K090891 · Microplex Coil System-Cosmos · MicroVention, Inc. · 2009 · recalled1990200020102020
Other ancestors, by generationDescendants, by generation 3 generations back: 1 other ancestor4 generations back: 4 other ancestors5 generations back: 7 other ancestors6 generations back: 18 other ancestors7 generations back: 1 other ancestor 1 generation forward: 3 descendants2 generations forward: 4 descendants3 generations forward: 1 descendant K090891 · Microplex Coil System-Cosmos · MicroVention, Inc. · 2009 · recalledK082461 · Bare Platinum Framing Coil, Model (S) 100408BPFC-V,100412BPFC-V,100515BPFC-V100518BPFC-V,100522BPFC-V,100618BPFC-V100622B · MicroVention, Inc. · 2008K050954 · Microplex Coil System (MCS) and Hydrocoil Embolic System (Hes) · MicroVention, Inc. · 2005 · recalledK041551 · Modification to: Hydrocoil Embolic System (Hes) · MicroVention, Inc. · 2004K033836 · Hydrocoil Embolic System (Hes) · MicroVention, Inc. · 2003K032590 · Microplex Coil System (MCS), Hydrocoil Embolic System (Hes) · MicroVention, Inc. · 2003K020434 · Microplex Coil System (MCS) · MicroVention, Inc. · 2002K012145 · Microplex Coil System · MicroVention, Inc. · 2001K991139 · Guglielmi Detachable (GDC) · Boston Scientific, Target · 1999K971395 · 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 · 1995−10−50
  1. Root · 13 generations backK951256 Detachable Platinum Coil (Guglielmi Detachable Coil, GDC)Target Therapeutics · 1995
  2. 9 generations between
  3. 3 generations backK050954 Microplex Coil System (MCS) and Hydrocoil Embolic System (Hes)MicroVention, Inc. · 2005 · Recalled
  4. 2 generations backK082461 Bare Platinum Framing Coil, Model (S)…MicroVention, Inc. · 2008
  5. 1 generation backK090891 Microplex Coil System-CosmosMicroVention, Inc. · 2009 · Recalled
  6. This deviceK093919 Microplex Coil System-Cosmos Model 100933CSSR-V, 101036CSSR-V…MicroVention, Inc. · 2010
  7. Descendant · cites it directly · 7 of its ownK103758 Microplex Coil System- Cosmos 10, Hydrocoil System- Hydroframe 10MicroVention, Inc. · 2011 · Recalled
  8. Descendant · cites it directly · 4 of its ownK111451 Microplex Coil System-Vector Model 030606XXX-V, 030610XXX-V…MicroVention, Inc. · 2011
  9. Descendant · cites it directly · 2 of its ownK132952 Microplex Coil System (MCS), Hydrocoil Embolic System (Hes)MicroVention, Inc. · 2013 · Recalled
  10. Descendant · 2 generations on · 1 of its ownK153594 MicroPlex Coil System (MCS), Hydrocoil Embolic System (HES)MicroVention, Inc. · 2016 · Recalled
  11. Descendant · 2 generations on · 1 of its ownK131948 Microplex Coil System (MCS)MicroVention, Inc. · 2013 · Recalled
Show all 13 generations
  1. Root · 13 generations backK951256 Detachable Platinum Coil (Guglielmi Detachable Coil, GDC)Target Therapeutics · 1995
  2. 12 generations backK960705 Guglielmi Detachable CoilTarget Therapeutics · 1996
  3. 11 generations backK962503 Guglielmi Detachable CoilTarget Therapeutics · 1996
  4. 10 generations backK971395 Guglielmi Detachable Coil (GDC), Fibered Platinum Coil, .035 Type…Target Therapeutics · 1997
  5. 9 generations backK991139 Guglielmi Detachable (GDC)Boston Scientific, Target · 1999
  6. 8 generations backK012145 Microplex Coil SystemMicroVention, Inc. · 2001
  7. 7 generations backK020434 Microplex Coil System (MCS)MicroVention, Inc. · 2002
  8. 6 generations backK032590 Microplex Coil System (MCS), Hydrocoil Embolic System (Hes)MicroVention, Inc. · 2003
  9. 5 generations backK033836 Hydrocoil Embolic System (Hes)MicroVention, Inc. · 2003
  10. 4 generations backK041551 Modification to: Hydrocoil Embolic System (Hes)MicroVention, Inc. · 2004
  11. 3 generations backK050954 Microplex Coil System (MCS) and Hydrocoil Embolic System (Hes)MicroVention, Inc. · 2005 · Recalled
  12. 2 generations backK082461 Bare Platinum Framing Coil, Model (S)…MicroVention, Inc. · 2008
  13. 1 generation backK090891 Microplex Coil System-CosmosMicroVention, Inc. · 2009 · Recalled
  14. This deviceK093919 Microplex Coil System-Cosmos Model 100933CSSR-V, 101036CSSR-V…MicroVention, Inc. · 2010

Showing 5 of 8 descendants. See all descendants

Descendants cleared per year

2011: 22013: 32016: 3
2011high 3 (2013) · low 0 (2012)2026

Most influential descendants

Showing 5 of 8 · See all
  • K103758Microplex Coil System- Cosmos 10, Hydrocoil System- Hydroframe 10MicroVention, Inc. · 2011 · cites it directly7descendants
  • K111451Microplex Coil System-Vector Model 030606XXX-V, 030610XXX-V, 30615XXX-V, 061020XXX-V…MicroVention, Inc. · 2011 · cites it directly4descendants
  • K132952Microplex Coil System (MCS), Hydrocoil Embolic System (Hes)MicroVention, Inc. · 2013 · cites it directly2descendants
  • K153594MicroPlex Coil System (MCS), Hydrocoil Embolic System (HES)MicroVention, Inc. · 2016 · 2 generations on1descendant
  • K131948Microplex Coil System (MCS)MicroVention, Inc. · 2013 · 2 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−13K951256Detachable Platinum Coil (Guglielmi Detachable Coil, GDC)Target Therapeutics1995—
−12K960705Guglielmi Detachable CoilTarget Therapeutics1996—
−11K962503Guglielmi Detachable CoilTarget Therapeutics1996—
−10K971395Guglielmi Detachable Coil (GDC), Fibered Platinum Coil, .035 Type, Berenstein…Target Therapeutics1997—
−9K991139Guglielmi Detachable (GDC)Boston Scientific, Target1999—
−8K012145Microplex Coil SystemMicroVention, Inc.2001—
−7K020434Microplex Coil System (MCS)MicroVention, Inc.2002—
−6K032590Microplex Coil System (MCS), Hydrocoil Embolic System (Hes)MicroVention, Inc.2003—
−5K033836Hydrocoil Embolic System (Hes)MicroVention, Inc.2003—
−4K041551Modification to: Hydrocoil Embolic System (Hes)MicroVention, Inc.2004—
−3K050954Microplex Coil System (MCS) and Hydrocoil Embolic System (Hes)MicroVention, Inc.200516
−2K082461Bare Platinum Framing Coil, Model (S)…MicroVention, Inc.2008—
−1K090891Microplex Coil System-CosmosMicroVention, Inc.20092
0 (this device)K093919Microplex Coil System-Cosmos Model 100933CSSR-V, 101036CSSR-V, 101141CSSR-V…MicroVention, Inc.2010—
+1K103758Microplex Coil System- Cosmos 10, Hydrocoil System- Hydroframe 10MicroVention, Inc.20111
+1K111451Microplex Coil System-Vector Model 030606XXX-V, 030610XXX-V, 30615XXX-V…MicroVention, Inc.2011—
+1K132952Microplex Coil System (MCS), Hydrocoil Embolic System (Hes)MicroVention, Inc.201316
+2K153594MicroPlex Coil System (MCS), Hydrocoil Embolic System (HES)MicroVention, Inc.201616
+2K131948Microplex Coil System (MCS)MicroVention, Inc.201311

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198610
198830
198910
199010
199120
199250
199430
199520
199620
199710
200040
200110
200220
200330

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201120
201330
201630
FIG. 1 — Lineage of K093919, 1995–2016Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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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.

Planning a device in HCG? 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? (2)

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
*K082461Bare Platinum Framing Coil, Model (S)…
Summary page 1
…Tustin, California 92780 U.S.A. Contact: Laraine Pangelina Predicate Device: Micro~lex Coil System (MCS) - Cosmos (K082461 and .K090891) Device Description: The Cosmos consist of an implant coil made of platinum alloy…
MicroVention, Inc.2008—
*K090891Microplex Coil System-Cosmos
Summary page 1
…U.S.A. Contact: Laraine Pangelina Predicate Device: Micro~lex Coil System (MCS) - Cosmos (K082461 and .K090891) Device Description: The Cosmos consist of an implant coil made of platinum alloy TIhe coils are desig…
MicroVention, Inc.20092

Also cleared against K082461: 3 other devices →

What descends from it? (8)

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

NumberDeviceApplicantDecidedDescendants
K103758Microplex Coil System- Cosmos 10, Hydrocoil System- Hydroframe 10MicroVention, Inc.20117
K111451Microplex Coil System-Vector Model 030606XXX-V, 030610XXX-V, 30615XXX-V, 061020XXX-V…MicroVention, Inc.20114
K132952Microplex Coil System (MCS), Hydrocoil Embolic System (Hes)MicroVention, Inc.20132

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Nov 22, 2019Class IIZ-1398-2020Process designThe devices may be missing the implant coil.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 15 years and passes through 3 companies; a new generation was cleared every 9 months on median.
  • 9 of the 44 ancestors have a recall of any class.
  • Of its descendants, K103758 (MicroVention, Inc., 2011) has gone furthest, with 7 descendants of its own.
  • 3 other devices also cite its predicate K082461.

How does its category compare?

All HCG devices

HCG Device, Neurovascular Embolization: FDA decisions, review times, recalls and adverse event reports over 20 years. 2010, 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 MicroPlex Coil System is intended for the endovascular embolization of intracranial aneurysms and other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae. The MCS is also intended for vascular occlusion of blood vessels within the neurovascular system to permanently obstruct blood flow to an aneurysm or other vascular malformation and/or arterial and venous embolizations in the peripheral vasculature.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K093919: Microplex Coil System-Cosmos Model 100933CSSR-V, 101036CSSR-V, 101141CSSR-V, 101245CSSR-V.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K093919

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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