510(k) Report

510(k) · Cleared

Cleared

Barricade Embolization Coil System

K142513510(k) SpecialCleared Nov 13, 201466-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

Blockade Medical · HCG Device, Neurovascular Embolization

Cleared on Nov 13, 2014 as substantially equivalent to K132482 (Blockade Medical, 2013) and 3 other predicates after a 66-day review. Its family tree reaches back 20 generations to 1995. 11 later devices descend from it.

Decided
Nov 13, 2014
Review
66 days
Class
Class II
Product code
HCG
Recalls
None
Predicates
4

Its longest line of descent runs back 20 generations to K951256 (1995). 62 ancestors in all, the oldest K860840 (1986). 11 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2011: 1 other ancestor2010: 2 other ancestors2009: 2 other ancestors2005: 1 other ancestor2004: 1 other ancestor2003: 4 other ancestors2002: 3 other ancestors2000: 5 other ancestors2008: 1 other ancestor1994: 3 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 ancestor1990: 1 other ancestor2001: 1 other ancestor2015: 1 descendant cleared2018: 1 descendant cleared2020: 2 descendants cleared2021: 1 descendant cleared2022: 2 descendants cleared2025: 2 descendants cleared2024: 1 descendant cleared2026: 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 · 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 · recalledK070656 · Hydrocoil Embolic System (Hes) · MicroVention, Inc. · 2007K080666 · Hydrosoft and Hydrosoft Plus Embolization Coil Systems · MicroVention, Inc. · 2008×3: 3 generations cleared close together, K112226 (2011), K113457 (2011), K120908 (2012) ×4: 4 generations cleared close together, K123338 (2013), K131475 (2013), K132482 (2013), K140104 (2014) 1990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 3 other ancestors3 generations back: 6 other ancestors4 generations back: 6 other ancestors5 generations back: 2 other ancestors6 generations back: 19 other ancestors7 generations back: 4 other ancestors8 generations back: 1 other ancestor9 generations back: 1 other ancestor 1 generation forward: 1 descendant2 generations forward: 2 descendants3 generations forward: 2 descendants4 generations forward: 2 descendants5 generations forward: 2 descendants6 generations forward: 1 descendant7 generations forward: 1 descendant K140104 · Barricade Embolization Coil System · Blockade Medical · 2014K132482 · Barricade Embolization Coil System · Blockade Medical · 2013K131475 · Barricade Embolization Coil System · Blockade Medical · 2013K123338 · Barricade Embolization Coil System · Blockade Medical · 2013K120908 · Hydrocoil Embolic System (Hes) · MicroVention, Inc. · 2012K113457 · Hydrocoil Embolic System (Hes) · MicroVention, Inc. · 2011K112226 · Hydrocoil Embolic System (Hes) · MicroVention, Inc. · 2011K080666 · Hydrosoft and Hydrosoft Plus Embolization Coil Systems · MicroVention, Inc. · 2008K070656 · Hydrocoil Embolic System (Hes) · MicroVention, Inc. · 2007K050954 · 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 · 1995−20−15−10−50+5
  1. Root · 20 generations backK951256 Detachable Platinum Coil (Guglielmi Detachable Coil, GDC)Target Therapeutics · 1995
  2. 16 generations between
  3. 3 generations backK131475 Barricade Embolization Coil SystemBlockade Medical · 2013
  4. 2 generations backK132482 Barricade Embolization Coil SystemBlockade Medical · 2013
  5. 1 generation backK140104 Barricade Embolization Coil SystemBlockade Medical · 2014
  6. This deviceK142513 Barricade Embolization Coil SystemBlockade Medical · 2014
  7. Descendant · cites it directly · 10 of its ownK151760 Barricade Embolization Coil SystemBlockade Medical · 2015
  8. Descendant · 2 generations on · 7 of its ownK172390 Optima Coil SystemBlockade Medical, LLC (D.B.A. Balt Usa) · 2018 · Recalled
  9. Descendant · 3 generations on · 6 of its ownK200030 Optima Coil SystemBalt USA, LLC · 2020 · Recalled
  10. Descendant · 4 generations on · 3 of its ownK223386 Optima Coil SystemBalt USA, LLC · 2022 · Recalled
  11. Descendant · 5 generations on · 2 of its ownK242582 Optima Coil System (OptiBlock Line Extension)Balt USA, LLC · 2024
Show all 20 generations
  1. Root · 20 generations backK951256 Detachable Platinum Coil (Guglielmi Detachable Coil, GDC)Target Therapeutics · 1995
  2. 19 generations backK960705 Guglielmi Detachable CoilTarget Therapeutics · 1996
  3. 18 generations backK962503 Guglielmi Detachable CoilTarget Therapeutics · 1996
  4. 17 generations backK971395 Guglielmi Detachable Coil (GDC), Fibered Platinum Coil, .035 Type…Target Therapeutics · 1997
  5. 16 generations backK991139 Guglielmi Detachable (GDC)Boston Scientific, Target · 1999
  6. 15 generations backK012145 Microplex Coil SystemMicroVention, Inc. · 2001
  7. 14 generations backK020434 Microplex Coil System (MCS)MicroVention, Inc. · 2002
  8. 13 generations backK032590 Microplex Coil System (MCS), Hydrocoil Embolic System (Hes)MicroVention, Inc. · 2003
  9. 12 generations backK033836 Hydrocoil Embolic System (Hes)MicroVention, Inc. · 2003
  10. 11 generations backK041551 Modification to: Hydrocoil Embolic System (Hes)MicroVention, Inc. · 2004
  11. 10 generations backK050954 Microplex Coil System (MCS) and Hydrocoil Embolic System (Hes)MicroVention, Inc. · 2005 · Recalled
  12. 9 generations backK070656 Hydrocoil Embolic System (Hes)MicroVention, Inc. · 2007
  13. 8 generations backK080666 Hydrosoft and Hydrosoft Plus Embolization Coil SystemsMicroVention, Inc. · 2008
  14. 7 generations backK112226 Hydrocoil Embolic System (Hes)MicroVention, Inc. · 2011
  15. 6 generations backK113457 Hydrocoil Embolic System (Hes)MicroVention, Inc. · 2011
  16. 5 generations backK120908 Hydrocoil Embolic System (Hes)MicroVention, Inc. · 2012
  17. 4 generations backK123338 Barricade Embolization Coil SystemBlockade Medical · 2013
  18. 3 generations backK131475 Barricade Embolization Coil SystemBlockade Medical · 2013
  19. 2 generations backK132482 Barricade Embolization Coil SystemBlockade Medical · 2013
  20. 1 generation backK140104 Barricade Embolization Coil SystemBlockade Medical · 2014
  21. This deviceK142513 Barricade Embolization Coil SystemBlockade Medical · 2014

Showing 5 of 11 descendants. See all descendants

Descendants cleared per year

2015: 12018: 12020: 22021: 12022: 22024: 12025: 22026: 1
2015high 2 (2020) · low 0 (2016)2026

Most influential descendants

Showing 5 of 11 · See all
  • K151760Barricade Embolization Coil SystemBlockade Medical · 2015 · cites it directly10descendants
  • K172390Optima Coil SystemBlockade Medical, LLC (D.B.A. Balt Usa) · 2018 · 2 generations on7descendants
  • K200030Optima Coil SystemBalt USA, LLC · 2020 · 3 generations on6descendants
  • K223386Optima Coil SystemBalt USA, LLC · 2022 · 4 generations on3descendants
  • K242582Optima Coil System (OptiBlock Line Extension)Balt USA, LLC · 2024 · 5 generations on2descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−20K951256Detachable Platinum Coil (Guglielmi Detachable Coil, GDC)Target Therapeutics1995—
−19K960705Guglielmi Detachable CoilTarget Therapeutics1996—
−18K962503Guglielmi Detachable CoilTarget Therapeutics1996—
−17K971395Guglielmi Detachable Coil (GDC), Fibered Platinum Coil, .035 Type, Berenstein…Target Therapeutics1997—
−16K991139Guglielmi Detachable (GDC)Boston Scientific, Target1999—
−15K012145Microplex Coil SystemMicroVention, Inc.2001—
−14K020434Microplex Coil System (MCS)MicroVention, Inc.2002—
−13K032590Microplex Coil System (MCS), Hydrocoil Embolic System (Hes)MicroVention, Inc.2003—
−12K033836Hydrocoil Embolic System (Hes)MicroVention, Inc.2003—
−11K041551Modification to: Hydrocoil Embolic System (Hes)MicroVention, Inc.2004—
−10K050954Microplex Coil System (MCS) and Hydrocoil Embolic System (Hes)MicroVention, Inc.200516
−9K070656Hydrocoil Embolic System (Hes)MicroVention, Inc.2007—
−8K080666Hydrosoft and Hydrosoft Plus Embolization Coil SystemsMicroVention, Inc.2008—
−7K112226Hydrocoil Embolic System (Hes)MicroVention, Inc.2011—
−6K113457Hydrocoil Embolic System (Hes)MicroVention, Inc.2011—
−5K120908Hydrocoil Embolic System (Hes)MicroVention, Inc.2012—
−4K123338Barricade Embolization Coil SystemBlockade Medical2013—
−3K131475Barricade Embolization Coil SystemBlockade Medical2013—
−2K132482Barricade Embolization Coil SystemBlockade Medical2013—
−1K140104Barricade Embolization Coil SystemBlockade Medical2014—
0 (this device)K142513Barricade Embolization Coil SystemBlockade Medical2014—
+1K151760Barricade Embolization Coil SystemBlockade Medical2015—
+2K172390Optima Coil SystemBlockade Medical, LLC (D.B.A. Balt Usa)20184
+3K200030Optima Coil SystemBalt USA, LLC20205
+4K223386Optima Coil SystemBalt USA, LLC20221
+5K242582Optima Coil System (OptiBlock Line Extension)Balt USA, LLC2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198610
198830
198910
199010
199120
199250
199430
199520
199620
199710
200050
200110
200230
200340
200410
200510
200810
200920
201020
201110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201510
201810
202020
202110
202220
202410
202520
202610
FIG. 1 — Lineage of K142513, 1995–2026Source: 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? (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
*K132482Barricade Embolization Coil System
Our reading of the summary gave K134482, which is not a number in FDA’s lists. Corrected to the number one digit away whose FDA name carries the summary’s words for the device, “Barricade Embolization Coil System”.
Blockade Medical2013—
*K131475Barricade Embolization Coil System
Summary page 4
…E Class 2, per 21 CFR 882.5950 CLASSIFICATION: PRODUCT CODE HCG PREDICATE DEVICES: Barricade Embolization Coil System (K134482, K131475, K123338, K140104) Substantially Equivalent To: The modified Barricade Embolization Coil System is substan…
Blockade Medical2013—
*K123338Barricade Embolization Coil System
Summary page 4
…er 21 CFR 882.5950 CLASSIFICATION: PRODUCT CODE HCG PREDICATE DEVICES: Barricade Embolization Coil System (K134482, K131475, K123338, K140104) Substantially Equivalent To: The modified Barricade Embolization Coil System is substantially equivalent in intended u…
Blockade Medical2013—
*K140104Barricade Embolization Coil System
Summary page 4
…882.5950 CLASSIFICATION: PRODUCT CODE HCG PREDICATE DEVICES: Barricade Embolization Coil System (K134482, K131475, K123338, K140104) Substantially Equivalent To: The modified Barricade Embolization Coil System is substantially equivalent in intended use, princ…
Blockade Medical2014—

Also cleared against K132482: 2 other devices →

What descends from it? (11)

See all 11

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K151760Barricade Embolization Coil SystemBlockade Medical201510

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

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 19 years and passes through 4 companies; a new generation was cleared every 9 months on median.
  • 13 of the 62 ancestors have a recall of any class.
  • Of its descendants, K151760 (Blockade Medical, 2015) has gone furthest, with 10 descendants of its own.
  • 2 other devices also cite its predicate K132482.

How does its category compare?

All HCG devices

HCG Device, Neurovascular Embolization: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, 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 Barricade Coil System (BCS) is intended for the endovascular embolization of intracranial aneurysms and other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae. The BCS 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 for arterial and venous embolizations in the peripheral vasculature.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K142513: Barricade Embolization Coil System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K142513

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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