510(k) Report

510(k) · Cleared

Recalled · Class II · 2022

VADER®one Pedicle System MIS and LightMore® Pedicle System 6.0

K193423510(k) TraditionalCleared May 22, 2020165-day reviewClass II21 CFR 888.3070Recalls 1

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

Icotec AG · NKB Thoracolumbosacral Pedicle Screw System

Cleared on May 22, 2020 as substantially equivalent to K190545 (Icotec AG, 2019) and 4 other predicates after a 165-day review. Its family tree reaches back 18 generations to 2004. 6 later devices descend from it. It has been recalled once.

Decided
May 22, 2020
Review
165 days
Class
Class II
Product code
NKB
Recalls
1
Predicates
6

Its longest line of descent runs back 18 generations to K040583 (2004). 273 ancestors in all, the oldest K841189 (1984). 6 later devices descend from it, 3 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2016: 3 other ancestors2012: 3 other ancestors2008: 11 other ancestors2013: 1 other ancestor2011: 6 other ancestors2007: 12 other ancestors2005: 20 other ancestors1999: 16 other ancestors2017: 1 other ancestor2010: 11 other ancestors2009: 10 other ancestors2006: 18 other ancestors2004: 27 other ancestors2003: 18 other ancestors2002: 16 other ancestors2001: 18 other ancestors2000: 17 other ancestors1998: 12 other ancestors1997: 7 other ancestors2015: 1 other ancestor1996: 7 other ancestors1995: 6 other ancestors1994: 3 other ancestors1993: 2 other ancestors1992: 5 other ancestors1990: 2 other ancestors1985: 1 other ancestor1984: 1 other ancestor2023: 1 descendant cleared2025: 1 descendant cleared2024: 4 descendants clearedReference device: K172480 · icotec Interbody Cage System · Icotec AG · 2018×7: 7 generations cleared close together, K040583 (2004), K041118 (2004), K042025 (2004), K043151 (2005), K050809 (2005), K052187 (2005), K053101 (2006) ×2: 2 generations cleared close together, K091442 (2009), K091974 (2009) K102555 · CD Horizon Spinal System · Medtronic Sofamor Danek USA, Inc. · 2010×2: 2 generations cleared close together, K112473 (2011), K113174 (2011) K152604 · KYPHON HV-R Fenestrated Screw Cement, CD HORIZON Fenestrated Screw Set · Medtronic Sofamor Danek USA, Incorporated · 2016×2: 2 generations cleared close together, K160879 (2016), K170543 (2017) ×2: 2 generations cleared close together, K173487 (2018), K182377 (2018) K190545 · VADER® one Pedicle System MIS and LightMore® Pedicle System 6.0 · Icotec AG · 2019 · recalled19801990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 3 other ancestors2 generations back: 9 other ancestors3 generations back: 41 other ancestors4 generations back: 58 other ancestors5 generations back: 61 other ancestors6 generations back: 37 other ancestors7 generations back: 25 other ancestors8 generations back: 13 other ancestors9 generations back: 8 other ancestors 1 generation forward: 3 descendants2 generations forward: 3 descendants K190545 · VADER® one Pedicle System MIS and LightMore® Pedicle System 6.0 · Icotec AG · 2019 · recalledK182377 · CarboClear® Pedicle Screw System · CarboFix Orthopedics, Ltd. · 2018K173487 · CarboClear® Pedicle Screw System · CarboFix Orthopedics, Ltd. · 2018K170543 · VIPER PRIME™ Screws with Fenestrations · Medos International SARL · 2017K160879 · CONFIDENCE™ High Viscosity Spinal Cement, VIPER® and EXPEDIUM® Fenestrated Screw Systems · Medos International Sàrl · 2016K152604 · KYPHON HV-R Fenestrated Screw Cement, CD HORIZON Fenestrated Screw Set · Medtronic Sofamor Danek USA, Incorporated · 2016K113174 · CD Horizon Spinal System · Medtronic Sofamor Danek USA, Inc. · 2011 · recalledK112473 · CD Horizon Spinal System · Medtronic Sofamor Danek, Inc. · 2011K102555 · CD Horizon Spinal System · Medtronic Sofamor Danek USA, Inc. · 2010K091974 · Modification to CD Horizon Spinal System · Medtronic Sofamor Danek USA, Inc. · 2009 · recalledK091442 · CD Horizon Spinal System · Medtronic Sofamor Danek · 2009K053101 · CD Horizon Spinal System · Medtronic Sofamor Danek · 2006K052187 · Modification to: CD Horizon Spinal System · Medtronic Sofamor Danek · 2005K050809 · CD Horizon Spinal System · Medtronic Sofamor Danek USA, Inc. · 2005K043151 · Modification to: CD Horizon Spinal System · Medtronic Sofamor Danek · 2005K042025 · Modification to CD Horizon Spinal System · Medtronic Sofamor Danek, Inc. · 2004 · recalledK041118 · Modification to CD Horizon Spinal System · Medtronic Sofamor Danek · 2004K040583 · Modification to: CD Horizon Spinal System · Medtronic Sofamor Danek · 2004−15−10−50
  1. Root · 18 generations backK040583 Modification to: CD Horizon Spinal SystemMedtronic Sofamor Danek · 2004
  2. 14 generations between
  3. 3 generations backK173487 CarboClear® Pedicle Screw SystemCarboFix Orthopedics, Ltd. · 2018
  4. 2 generations backK182377 CarboClear® Pedicle Screw SystemCarboFix Orthopedics, Ltd. · 2018
  5. 1 generation backK190545 VADER® one Pedicle System MIS and LightMore® Pedicle System 6.0Icotec AG · 2019 · Recalled
  6. This deviceK193423 VADER®one Pedicle System MIS and LightMore® Pedicle System 6.0Icotec AG · 2020
  7. Descendant · cites it directly · 4 of its ownK231280 CarboClear® X Pedicle Screw System; CarboClear® X Navigated…CarboFix Orthopedics, Ltd. · 2023
  8. Descendant · 2 generations on · 3 of its ownK233944 CarboClear® X Pedicle Screw System; CarboClear® X Navigated…CarboFix Orthopedics, Ltd. · 2024
  9. Descendant · cites it directly · 2 of its ownK240846 CarboClear® Hybrid Pedicle Screw System; CarboClear® Hybrid…CarboFix Orthopedics, Ltd. · 2024
  10. Descendant · 2 generations on · 1 of its ownK233793 CarboClear® X Pedicle Screw SystemCarboFix Orthopedics, Ltd. · 2024
  11. Descendant · cites it directly · 0 of its ownK242900 VADER® Pedicle System and VADER®one Pedicle SystemIcotec AG · 2025
Show all 18 generations
  1. Root · 18 generations backK040583 Modification to: CD Horizon Spinal SystemMedtronic Sofamor Danek · 2004
  2. 17 generations backK041118 Modification to CD Horizon Spinal SystemMedtronic Sofamor Danek · 2004
  3. 16 generations backK042025 Modification to CD Horizon Spinal SystemMedtronic Sofamor Danek, Inc. · 2004 · Recalled
  4. 15 generations backK043151 Modification to: CD Horizon Spinal SystemMedtronic Sofamor Danek · 2005
  5. 14 generations backK050809 CD Horizon Spinal SystemMedtronic Sofamor Danek USA, Inc. · 2005
  6. 13 generations backK052187 Modification to: CD Horizon Spinal SystemMedtronic Sofamor Danek · 2005
  7. 12 generations backK053101 CD Horizon Spinal SystemMedtronic Sofamor Danek · 2006
  8. 11 generations backK091442 CD Horizon Spinal SystemMedtronic Sofamor Danek · 2009
  9. 10 generations backK091974 Modification to CD Horizon Spinal SystemMedtronic Sofamor Danek USA, Inc. · 2009 · Recalled
  10. 9 generations backK102555 CD Horizon Spinal SystemMedtronic Sofamor Danek USA, Inc. · 2010
  11. 8 generations backK112473 CD Horizon Spinal SystemMedtronic Sofamor Danek, Inc. · 2011
  12. 7 generations backK113174 CD Horizon Spinal SystemMedtronic Sofamor Danek USA, Inc. · 2011 · Recalled
  13. 6 generations backK152604 KYPHON HV-R Fenestrated Screw Cement, CD HORIZON Fenestrated Screw SetMedtronic Sofamor Danek USA, Incorporated · 2016
  14. 5 generations backK160879 CONFIDENCE™ High Viscosity Spinal Cement, VIPER® and EXPEDIUM®…Medos International Sàrl · 2016
  15. 4 generations backK170543 VIPER PRIME™ Screws with FenestrationsMedos International SARL · 2017
  16. 3 generations backK173487 CarboClear® Pedicle Screw SystemCarboFix Orthopedics, Ltd. · 2018
  17. 2 generations backK182377 CarboClear® Pedicle Screw SystemCarboFix Orthopedics, Ltd. · 2018
  18. 1 generation backK190545 VADER® one Pedicle System MIS and LightMore® Pedicle System 6.0Icotec AG · 2019 · Recalled
  19. This deviceK193423 VADER®one Pedicle System MIS and LightMore® Pedicle System 6.0Icotec AG · 2020

Showing 5 of 6 descendants. See all descendants

Descendants cleared per year

2023: 12024: 42025: 1
2023high 4 (2024) · low 0 (2026)2026

Most influential descendants

Showing 5 of 6 · See all
  • K231280CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments; CarboClear® X…CarboFix Orthopedics, Ltd. · 2023 · cites it directly4descendants
  • K233944CarboClear® X Pedicle Screw System; CarboClear® X Navigated InstrumentsCarboFix Orthopedics, Ltd. · 2024 · 2 generations on3descendants
  • K240846CarboClear® Hybrid Pedicle Screw System; CarboClear® Hybrid Navigated Instruments…CarboFix Orthopedics, Ltd. · 2024 · cites it directly2descendants
  • K233793CarboClear® X Pedicle Screw SystemCarboFix Orthopedics, Ltd. · 2024 · 2 generations on1descendant
  • K242900VADER® Pedicle System and VADER®one Pedicle SystemIcotec AG · 2025 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−18K040583Modification to: CD Horizon Spinal SystemMedtronic Sofamor Danek2004—
−17K041118Modification to CD Horizon Spinal SystemMedtronic Sofamor Danek2004—
−16K042025Modification to CD Horizon Spinal SystemMedtronic Sofamor Danek, Inc.20044
−15K043151Modification to: CD Horizon Spinal SystemMedtronic Sofamor Danek2005—
−14K050809CD Horizon Spinal SystemMedtronic Sofamor Danek USA, Inc.2005—
−13K052187Modification to: CD Horizon Spinal SystemMedtronic Sofamor Danek2005—
−12K053101CD Horizon Spinal SystemMedtronic Sofamor Danek2006—
−11K091442CD Horizon Spinal SystemMedtronic Sofamor Danek2009—
−10K091974Modification to CD Horizon Spinal SystemMedtronic Sofamor Danek USA, Inc.20091
−9K102555CD Horizon Spinal SystemMedtronic Sofamor Danek USA, Inc.2010—
−8K112473CD Horizon Spinal SystemMedtronic Sofamor Danek, Inc.2011—
−7K113174CD Horizon Spinal SystemMedtronic Sofamor Danek USA, Inc.20111
−6K152604KYPHON HV-R Fenestrated Screw Cement, CD HORIZON Fenestrated Screw SetMedtronic Sofamor Danek USA, Incorporated2016—
−5K160879CONFIDENCE™ High Viscosity Spinal Cement, VIPER® and EXPEDIUM® Fenestrated…Medos International Sàrl2016—
−4K170543VIPER PRIME™ Screws with FenestrationsMedos International SARL2017—
−3K173487CarboClear® Pedicle Screw SystemCarboFix Orthopedics, Ltd.2018—
−2K182377CarboClear® Pedicle Screw SystemCarboFix Orthopedics, Ltd.2018—
−1K190545VADER® one Pedicle System MIS and LightMore® Pedicle System 6.0Icotec AG20191
0 (this device)K193423VADER®one Pedicle System MIS and LightMore® Pedicle System 6.0Icotec AG2020—
+1K231280CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments…CarboFix Orthopedics, Ltd.2023—
+2K233944CarboClear® X Pedicle Screw System; CarboClear® X Navigated InstrumentsCarboFix Orthopedics, Ltd.2024—
+1K240846CarboClear® Hybrid Pedicle Screw System; CarboClear® Hybrid Navigated…CarboFix Orthopedics, Ltd.2024—
+2K233793CarboClear® X Pedicle Screw SystemCarboFix Orthopedics, Ltd.2024—
+1K242900VADER® Pedicle System and VADER®one Pedicle SystemIcotec AG2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198410
198510
199020
199250
199320
199430
199560
199670
199770
1998120
1999160
2000170
2001180
2002160
2003180
2004270
2005200
2006180
2007120
2008110
2009100
2010110
201160
201230
201310
201510
201630
201710

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202310
202440
202510
FIG. 1 — Lineage of K193423, 2004–2025Source: 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 NKB? 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 NKB device

  1. #1 K223494 CD Horizon Spinal Systemscore 40.4 · 30 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? (6)

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; numbers the summary cites that cannot be its predicate are marked – and kept off the family tree.

TypeNumberDeviceApplicantDecidedRecalls
*K190545VADER® one Pedicle System MIS and LightMore® Pedicle System 6.0
Summary page 5
…VADER®one Pedicle System MIS and LightMore® Pedicle System 6.0 are substantially equivalent to the icotec VADER®one Pedicle System MIS and LightMore® Pedicle System 6.0 (K190545). Additional Predicate Devices: The VADER®one Pedicle System MIS and LightMore® Pedicle System 6.0 are substantially equivalent…
Icotec AG20191
*K151977icotec Pedicle System
Summary page 5
…Devices: The VADER®one Pedicle System MIS and LightMore® Pedicle System 6.0 are substantially equivalent to additional predicate devices: x icotec Pedicle System (K151977) x Blackstone Pedicle Screw System (K082797) x Corelink Tiger Spine System (K113058) x CarboFix Pedicle Screw Syst…
Icotec AG2016—
*K082797Blackstone Pedicle Screw System
Summary page 5
…ghtMore® Pedicle System 6.0 are substantially equivalent to additional predicate devices: x icotec Pedicle System (K151977) x Blackstone Pedicle Screw System (K082797) x Corelink Tiger Spine System (K113058) x CarboFix Pedicle Screw System (K182377) x Medtronic CD Horizon Astute S…
Blackstone Medical, Inc.2008—
*K113058Tiger Spine System
Summary page 5
…equivalent to additional predicate devices: x icotec Pedicle System (K151977) x Blackstone Pedicle Screw System (K082797) x Corelink Tiger Spine System (K113058) x CarboFix Pedicle Screw System (K182377) x Medtronic CD Horizon Astute Spinal System (K19066) Reference Device: The…
Corelink, LLC2012—
*K182377CarboClear® Pedicle Screw System
Summary page 5
…x icotec Pedicle System (K151977) x Blackstone Pedicle Screw System (K082797) x Corelink Tiger Spine System (K113058) x CarboFix Pedicle Screw System (K182377) x Medtronic CD Horizon Astute Spinal System (K19066) Reference Device: The subject 510(k) references the icotec Interbody…
CarboFix Orthopedics, Ltd.2018—
Kept off the family treeK190066Medtronic CD Horizon Astute Spinal System
Not matched in our reading of the summary (scans can blur digits), so it is kept off the family tree
†K172480icotec Interbody Cage SystemIcotec AG2018—

Also cleared against K190545: 3 other devices →

What descends from it? (6)

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

NumberDeviceApplicantDecidedDescendants
K231280CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments; CarboClear® X…CarboFix Orthopedics, Ltd.20234
K240846CarboClear® Hybrid Pedicle Screw System; CarboClear® Hybrid Navigated Instruments…CarboFix Orthopedics, Ltd.20242
K242900VADER® Pedicle System and VADER®one Pedicle SystemIcotec AG20250

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

Recalls of this device

DateClassRecallRoot causeReason
Nov 3, 2022Class IIZ-0728-2023Nonconforming Material/ComponentDuring internal testing (at manufacturer site) of two torque wrench devices, it was detected that the torque limiting function was out of specification. The specified torque limiting value is 12 Nm. The measuring results for both…

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 16 years and passes through 8 companies; a new generation was cleared every 5 months on median.
  • 31 of the 273 ancestors have a recall of any class.
  • Of its descendants, K231280 (CarboFix Orthopedics, Ltd., 2023) has gone furthest, with 4 descendants of its own.
  • 3 other devices also cite its predicate K190545.

How does its category compare?

All NKB devices

NKB Thoracolumbosacral Pedicle Screw System: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · NKB

24in 2025

2007: 382008: 362009: 442010: 372011: 482012: 602013: 352014: 462015: 552016: 502017: 632018: 562019: 392020: 482021: 322022: 342023: 442024: 392025: 242026 (partial year): 30
2007high 63 (2017) · low 24 (2025)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NKB

61in 2025

2007: 87 days median2008: 59 days median2009: 71 days median2010: 111 days median2011: 84 days median2012: 79 days median2013: 73 days median2014: 90 days median2015: 90 days median2016: 84 days median2017: 69 days median2018: 61 days median2019: 84 days median2020: 68 days median2021: 61 days median2022: 88 days median2023: 72 days median2024: 57 days median2025: 61 days median2026 (partial year): 91 days median
2007high 111 (2010) · low 57 (2024)2026

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

Recalls per year · NKB

1in 2025

2007: 42008: 52009: 332010: 42011: 32012: 132014: 3, 1 Class I2015: 32016: 12017: 12018: 32019: 12020: 12022: 52023: 22024: 32025: 12026 (partial year): 3
2007high 33 (2009) · low 0 (2013)2026

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

Adverse event reports per year · NKB

1,171in 2025

2007: 342008: 822009: 1712010: 4622011: 5772012: 1,7472013: 1,9622014: 1,6712015: 1,4462016: 1,5852017: 1,6182018: 1,6842019: 1,9152020: 2,0762021: 1,7452022: 1,3392023: 9192024: 1,6142025: 1,171
2007high 2,076 (2020) · low 34 (2007)2025

MAUDE reports naming product code NKB, 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
20073887434
20083659582
2009447133171
2010371114462
201148843577
20126079131,747
2013357301,962
201446903 (1)1,671
2015559031,446
2016508411,585
2017636911,618
2018566131,684
2019398411,915
2020486812,076
2021326101,745
2022348851,339
202344722919
2024395731,614
2025246111,171
202630913—

What is it indicated for?

The VADER®one Pedicle System MIS and LightMore® Pedicle System 6.0 are intended to restore the integrity of the spinal column even in the absence of fusion for a limited time period in patients with advanced stage tumors involving the thoracic and lumbar spine in whom life expectancy, prior to oncological treatment, is of insufficient duration to permit achievement of fusion.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K193423: VADER®one Pedicle System MIS and LightMore® Pedicle System 6.0.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K193423

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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