510(k) Report

510(k) · Cleared

Cleared

CD HORIZON Spinal System, Medtronic Navigated Manual Reusable Instruments for Use with the STEALTHSTATION System, Medtronic Reusable Instruments for Use with the IPC POWEREASE System, Medtronic Navigated Reusable Instruments for Use with the STEALTHSTATION and IPC POWEREASE Systems

K153442510(k) TraditionalCleared Feb 18, 201683-day reviewClass II21 CFR 888.3070

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

Medtronic Sofamor Danek USA, Inc. · NKB Thoracolumbosacral Pedicle Screw System

Cleared on Feb 18, 2016 as substantially equivalent to K113174 (Medtronic Sofamor Danek USA, Inc., 2011) and 8 other predicates after an 83-day review. Its family tree reaches back 14 generations to 1985. 84 later devices descend from it.

Decided
Feb 18, 2016
Review
83 days
Class
Class II
Product code
NKB
Recalls
None
Predicates
9

Its longest line of descent runs back 14 generations to K853033 (1985). 248 ancestors in all, the oldest K841189 (1984). 84 later devices descend from it, 13 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2015: 2 other ancestors2014: 4 other ancestors2013: 3 other ancestors2011: 6 other ancestors2010: 5 other ancestors2005: 22 other ancestors2009: 5 other ancestors2008: 11 other ancestors2006: 13 other ancestors2004: 29 other ancestors2007: 8 other ancestors2003: 15 other ancestors2002: 13 other ancestors2001: 21 other ancestors2000: 13 other ancestors1999: 12 other ancestors1997: 6 other ancestors1996: 7 other ancestors1994: 5 other ancestors1998: 11 other ancestors1995: 10 other ancestors1988: 2 other ancestors1987: 1 other ancestor1992: 2 other ancestors1989: 1 other ancestor1986: 2 other ancestors1984: 2 other ancestors1993: 1 other ancestor1985: 1 other ancestor1990: 1 other ancestor2022: 9 descendants cleared2018: 2 descendants cleared2025: 10 descendants cleared2023: 13 descendants cleared2016: 1 descendant cleared2024: 12 descendants cleared2021: 6 descendants cleared2020: 4 descendants cleared2017: 3 descendants cleared2019: 7 descendants cleared2026: 17 descendants clearedK853033 · Hartshill Rect & Wires, Spinal Fixation System · A.W. Showell (Surgicraft), Ltd. · 1985K965221 · Ransford Cervical Fixation System · Surgicraft, Ltd. · 1997K982322 · Synthes Spine Occipital-Cervical Plate/Rod and Hook System · Synthes (Usa) · 1998K002733 · Summit Occipito-Cervico-Thoracic (Oct) Spinal System · Depuyacromed · 2000K013222 · Summit Occipito-Cervico- Thoracic (Oct) Spinal System · Depuyacromed · 2001K022190 · Modification to Summit Occipito-Cervico-Thoracic (Oct) Spinal System · Depuyacromed · 2002K030103 · Summit Oct Spinal System Minipolyaxial Screws · Depuyacromed · 2003K041203 · Summit Oct Spinal System · Depuy Spine, Inc. · 2004×3: 3 generations cleared close together, K062174 (2006), K063156 (2006), K063741 (2007) K080313 · Modification to Expedium Spine System · Depuy Spine, Inc. · 2008K111571 · Viper Systems · Johnson & Johnson · 2011K121020 · Viper System · Depuy Spine, Inc. · 201219801990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 8 other ancestors2 generations back: 17 other ancestors3 generations back: 49 other ancestors4 generations back: 58 other ancestors5 generations back: 34 other ancestors6 generations back: 29 other ancestors7 generations back: 24 other ancestors8 generations back: 9 other ancestors9 generations back: 4 other ancestors10 generations back: 2 other ancestors 1 generation forward: 13 descendants2 generations forward: 16 descendants3 generations forward: 18 descendants4 generations forward: 14 descendants5 generations forward: 9 descendants6 generations forward: 13 descendants7 generations forward: 1 descendant K121020 · Viper System · Depuy Spine, Inc. · 2012K111571 · Viper Systems · Johnson & Johnson · 2011K080313 · Modification to Expedium Spine System · Depuy Spine, Inc. · 2008K063741 · Expedium Spine System · Depuy Spine, Inc. · 2007K063156 · Modification to Expedium Spine System · Depuy Spine, Inc. · 2006K062174 · Modification to Expedium Spine System · Depuy Spine, Inc. · 2006K041203 · Summit Oct Spinal System · Depuy Spine, Inc. · 2004K030103 · Summit Oct Spinal System Minipolyaxial Screws · Depuyacromed · 2003K022190 · Modification to Summit Occipito-Cervico-Thoracic (Oct) Spinal System · Depuyacromed · 2002K013222 · Summit Occipito-Cervico- Thoracic (Oct) Spinal System · Depuyacromed · 2001K002733 · Summit Occipito-Cervico-Thoracic (Oct) Spinal System · Depuyacromed · 2000K982322 · Synthes Spine Occipital-Cervical Plate/Rod and Hook System · Synthes (Usa) · 1998K965221 · Ransford Cervical Fixation System · Surgicraft, Ltd. · 1997K853033 · Hartshill Rect & Wires, Spinal Fixation System · A.W. Showell (Surgicraft), Ltd. · 1985−10−50+5
  1. Root · 14 generations backK853033 Hartshill Rect & Wires, Spinal Fixation SystemA.W. Showell (Surgicraft), Ltd. · 1985
  2. 10 generations between
  3. 3 generations backK080313 Modification to Expedium Spine SystemDepuy Spine, Inc. · 2008
  4. 2 generations backK111571 Viper SystemsJohnson & Johnson · 2011
  5. 1 generation backK121020 Viper SystemDepuy Spine, Inc. · 2012
  6. This deviceK153442 CD HORIZON Spinal System, Medtronic Navigated Manual Reusable…Medtronic Sofamor Danek USA, Inc. · 2016
  7. Descendant · cites it directly · 48 of its ownK161014 NuVasive® Reline® SystemNu Vasive, Incorporated · 2016
  8. Descendant · 2 generations on · 39 of its ownK170126 NuVasive® Reline® 4.5-5.0 SystemNu Vasive, Incorporated · 2017
  9. Descendant · cites it directly · 20 of its ownK221244 CD Horizon™ Spinal SystemMedtronic · 2022
  10. Descendant · 2 generations on · 17 of its ownK223494 CD Horizon Spinal SystemMedtronic · 2023
  11. Descendant · 3 generations on · 13 of its ownK190636 NuVasive® Reline® 4.5-5.0 SystemNu Vasive, Incorporated · 2019
Show all 14 generations
  1. Root · 14 generations backK853033 Hartshill Rect & Wires, Spinal Fixation SystemA.W. Showell (Surgicraft), Ltd. · 1985
  2. 13 generations backK965221 Ransford Cervical Fixation SystemSurgicraft, Ltd. · 1997
  3. 12 generations backK982322 Synthes Spine Occipital-Cervical Plate/Rod and Hook SystemSynthes (Usa) · 1998
  4. 11 generations backK002733 Summit Occipito-Cervico-Thoracic (Oct) Spinal SystemDepuyacromed · 2000
  5. 10 generations backK013222 Summit Occipito-Cervico- Thoracic (Oct) Spinal SystemDepuyacromed · 2001
  6. 9 generations backK022190 Modification to Summit Occipito-Cervico-Thoracic (Oct) Spinal SystemDepuyacromed · 2002
  7. 8 generations backK030103 Summit Oct Spinal System Minipolyaxial ScrewsDepuyacromed · 2003
  8. 7 generations backK041203 Summit Oct Spinal SystemDepuy Spine, Inc. · 2004
  9. 6 generations backK062174 Modification to Expedium Spine SystemDepuy Spine, Inc. · 2006
  10. 5 generations backK063156 Modification to Expedium Spine SystemDepuy Spine, Inc. · 2006
  11. 4 generations backK063741 Expedium Spine SystemDepuy Spine, Inc. · 2007
  12. 3 generations backK080313 Modification to Expedium Spine SystemDepuy Spine, Inc. · 2008
  13. 2 generations backK111571 Viper SystemsJohnson & Johnson · 2011
  14. 1 generation backK121020 Viper SystemDepuy Spine, Inc. · 2012
  15. This deviceK153442 CD HORIZON Spinal System, Medtronic Navigated Manual Reusable…Medtronic Sofamor Danek USA, Inc. · 2016

Showing 5 of 84 descendants. See all descendants

Descendants cleared per year

2016: 12017: 32018: 22019: 72020: 42021: 62022: 92023: 132024: 122025: 102026: 17
2016high 17 (2026) · low 1 (2016)2026

Most influential descendants

Showing 5 of 84 · See all
  • K161014NuVasive® Reline® SystemNu Vasive, Incorporated · 2016 · cites it directly48descendants
  • K170126NuVasive® Reline® 4.5-5.0 SystemNu Vasive, Incorporated · 2017 · 2 generations on39descendants
  • K221244CD Horizon™ Spinal SystemMedtronic · 2022 · cites it directly20descendants
  • K223494CD Horizon Spinal SystemMedtronic · 2023 · 2 generations on17descendants
  • K190636NuVasive® Reline® 4.5-5.0 SystemNu Vasive, Incorporated · 2019 · 3 generations on13descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−14K853033Hartshill Rect & Wires, Spinal Fixation SystemA.W. Showell (Surgicraft), Ltd.1985—
−13K965221Ransford Cervical Fixation SystemSurgicraft, Ltd.1997—
−12K982322Synthes Spine Occipital-Cervical Plate/Rod and Hook SystemSynthes (Usa)1998—
−11K002733Summit Occipito-Cervico-Thoracic (Oct) Spinal SystemDepuyacromed2000—
−10K013222Summit Occipito-Cervico- Thoracic (Oct) Spinal SystemDepuyacromed2001—
−9K022190Modification to Summit Occipito-Cervico-Thoracic (Oct) Spinal SystemDepuyacromed2002—
−8K030103Summit Oct Spinal System Minipolyaxial ScrewsDepuyacromed2003—
−7K041203Summit Oct Spinal SystemDepuy Spine, Inc.2004—
−6K062174Modification to Expedium Spine SystemDepuy Spine, Inc.2006—
−5K063156Modification to Expedium Spine SystemDepuy Spine, Inc.2006—
−4K063741Expedium Spine SystemDepuy Spine, Inc.2007—
−3K080313Modification to Expedium Spine SystemDepuy Spine, Inc.2008—
−2K111571Viper SystemsJohnson & Johnson2011—
−1K121020Viper SystemDepuy Spine, Inc.2012—
0 (this device)K153442CD HORIZON Spinal System, Medtronic Navigated Manual Reusable Instruments for…Medtronic Sofamor Danek USA, Inc.2016—
+1K161014NuVasive® Reline® SystemNu Vasive, Incorporated2016—
+2K170126NuVasive® Reline® 4.5-5.0 SystemNu Vasive, Incorporated2017—
+1K221244CD Horizon™ Spinal SystemMedtronic2022—
+2K223494CD Horizon Spinal SystemMedtronic2023—
+3K190636NuVasive® Reline® 4.5-5.0 SystemNu Vasive, Incorporated2019—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198420
198510
198620
198710
198820
198910
199010
199220
199310
199450
1995100
199670
199760
1998110
1999120
2000130
2001210
2002130
2003150
2004290
2005220
2006130
200780
2008110
200950
201050
201160
201330
201440
201520

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201610
201730
201820
201970
202040
202160
202290
2023130
2024120
2025100
2026170
FIG. 1 — Lineage of K153442, 1985–2026Source: 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.

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? (9)

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
*K113174CD Horizon Spinal System
Summary page 9
…CFR 878.4820 Predicates There are 9 Predicates. CD HORIZON® Spinal System K113174, S.E. 11/21/2011 (Primary Predicate) K050439, S.E. 03/24/2005…
Medtronic Sofamor Danek USA, Inc.20111
*K050439CD Horizon Spinal System
Summary page 9
…CD HORIZON® Spinal System K113174, S.E. 11/21/2011 (Primary Predicate) K050439, S.E. 03/24/2005 K102555, S.E. 11/17/2010 K152457, S.E. 10/27…
Medtronic Sofamor Danek, Inc.2005—
*K102555CD Horizon Spinal System
Summary page 9
…K113174, S.E. 11/21/2011 (Primary Predicate) K050439, S.E. 03/24/2005 K102555, S.E. 11/17/2010 K152457, S.E. 10/27/2015 DePuy Spine Inc. -…
Medtronic Sofamor Danek USA, Inc.2010—
*K152457CD HORIZON Spinal System
Summary page 9
…rimary Predicate) K050439, S.E. 03/24/2005 K102555, S.E. 11/17/2010 K152457, S.E. 10/27/2015 DePuy Spine Inc. - VIPER K121020, S.E. 05/03…
Medtronic Sofamor Danek USA, Inc.2015—
*K121020Viper System
Summary page 9
…, S.E. 11/17/2010 K152457, S.E. 10/27/2015 DePuy Spine Inc. - VIPER K121020, S.E. 05/03/2012 Medtronic Navigated Instruments K150231, S.…
Depuy Spine, Inc.2012—
*K150231Navigated Disc Prep Instruments and CAPSTONE Trials
Summary page 9
…. - VIPER K121020, S.E. 05/03/2012 Medtronic Navigated Instruments K150231, S.E. 06/16/2015 IPC® POWEREASE® System K111520, S.E. 10/26/…
Medtronic Sofamor Danek USA, Inc.2015—
*K111520Ipc Powerease System
Summary page 9
…igated Instruments K150231, S.E. 06/16/2015 IPC® POWEREASE® System K111520, S.E. 10/26/2011 Medtronic Navigated Taps and Screwdrivers K…
Medtronic Xomed, Inc.20112
*K124004Navigated CD Horizon Solera Screwdrivers, Taps, Iliac Taps, Legacy Taps
Summary page 9
…K111520, S.E. 10/26/2011 Medtronic Navigated Taps and Screwdrivers K124004, S.E. 03/22/2013 K140454, S.E. 05/22/2014 The predicates have…
Medtronic Navigation, Inc.20131
*K140454Navigated CD Horizon Solera Screwdriver/Taps
Summary page 9
…Medtronic Navigated Taps and Screwdrivers K124004, S.E. 03/22/2013 K140454, S.E. 05/22/2014 The predicates have not been subject to a design related…
Medtronic Sofamor Danek USA, Inc.20141

Also cleared against K113174: 36 other devices →

What descends from it? (84)

See all 84

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

NumberDeviceApplicantDecidedDescendants
K161014NuVasive® Reline® SystemNu Vasive, Incorporated201648
K221244CD Horizon™ Spinal SystemMedtronic202220
K201251CarboClear Navigated InstrumentsCarboFix Orthopedics, Ltd.20209
K210716CarboClear X Pedicle Screw System, CarboClear X Navigated InstrumentsCarboFix Orthopedics, Ltd.20218
K233951CD Horizon ModuLeX Spinal System (Shanks, Head Assemblies, and Set Screw)Medtronic Sofamor Danek USA, Inc.20245
K162921Navigated Instrument SystemOrthofix, Inc.20175
K172115Navigated Instrument SystemOrthofix, Inc.20184
K240846CarboClear® Hybrid Pedicle Screw System; CarboClear® Hybrid Navigated Instruments…CarboFix Orthopedics, Ltd.20242
K252322SIros-X SystemGenesys Spine20250
K223301ASTRA & AVANT Navigation Instruments System and ASTRA-OCT Navigation Instruments SystemSpinecraft, LLC20230

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 31 years and passes through 7 companies; a new generation was cleared every 1.3 years on median.
  • 27 of the 248 ancestors have a recall of any class.
  • Of its descendants, K161014 (Nu Vasive, Incorporated, 2016) has gone furthest, with 48 descendants of its own.
  • 36 other devices also cite its predicate K113174.

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. 2016, 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 CD HORIZON® Spinal System with or without SEXTANT® instrumentation is intended for posterior, non-cervical fixation as an adjunct to fusion for the following indications: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), spinal stenosis, curvatures (i.e., scoliosis, kyphosis, or lordosis), tumor…

Read the full statement (645 words)

The CD HORIZON® Spinal System with or without SEXTANT® instrumentation is intended for posterior, non-cervical fixation as an adjunct to fusion for the following indications: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), spinal stenosis, curvatures (i.e., scoliosis, kyphosis, or lordosis), tumor, pseudarthrosis, and/or failed previous fusion. Except for hooks, when used as an anterolateral thoracic/lumbar system, the CD HORIZON® Spinal System may also be used for the same indications as an adjunct to fusion.

With the exception of degenerative disc disease, the CD HORIZON® LEGACY™ 3.5mm rods and the CD HORIZON® Spinal System PEEK rods and associated components may be used for the aforementioned indications in skeletally mature patients as an adjunct to fusion. The 3.5mm rods may be used for the specific pediatric indications noted below.

When used for posterior non-cervical pedicle screw fixation in pediatric patients, the CD HORIZON® Spinal System implants are indicated as an adjunct to fusion to treat progressive spinal deformities (i.e., scoliosis, kyphosis, or lordosis) including idiopathic scoliosis, neuromuscular scoliosis, and congenital scoliosis. Additionally, the CD HORIZON® Spinal System is intended to treat pediatric patients diagnosed with the following conditions: spondylolisthesis/spondylolysis, fracture caused by tumor and/or trauma, pseudarthrosis, and/or failed previous fusion. These devices are to be used with autograft and/or allograft. Pediatric pedicle screw fixation is limited to a posterior approach.

The CD HORIZON® SPIRE™ Plate is a posterior, single-level, non-pedicle supplemental fixation device intended for use in the non-cervical spine (T1-S1) as an adjunct to fusion in skeletally mature patients. It is intended for plate fixation/attachment to spinous processes for the purpose of achieving supplemental fixation in the following conditions: degenerative disc disease (as previously defined), spondylolisthesis, trauma, and/or tumor.

In order to achieve additional levels of fixation, the CD HORIZON® Spinal System rods may be connected to the VERTEX® Reconstruction System with the VERTEX® rod connector. Refer to the VERTEX® Reconstruction System Package Insert for a list of the VERTEX® indications of use.

The Navigated Disc Preparation Instruments are intended to be used to facilitate a discectomy during spinal surgery. The Navigated Trials are intended to be used to facilitate implant size selection of Medtronic intervertebral body fusion devices during spinal surgery.

The Navigated Probe is intended to be used during pedicle and disc preparation during spinal fusion procedures.

Navigated instruments are specifically designed for use with the StealthStation® System, which is indicated for any medical condition in which the use of stereotactic surgery may be appropriate, and where reference to a rigid anatomical structure, such as a skull, a long bone, or vertebra, can be identified relative to a CT or MR based model, fluoroscopy images, or digitized landmarks of the anatomy.

IPC® System is indicated for the incision/cutting, removal, drilling and sawing of soft and hard tissue and bone, and biomaterials in Neurosurgical (Cranial, Craniofacial), Orthopedic, Arthroscopic, Spinal, Sternotomy, and General surgical procedures.

The IPC® POWEREASE® System is indicated for drilling, tapping and driving screws and working end attachments during spinal surgery, including open and minimally invasive procedures. It is also used in placement or cutting of screws, posts and rods.

Medtronic Navigated Reusable Instruments are intended to be used during the preparation and placement of Medtronic screws during spinal surgery to assist the surgeon in precisely locating anatomical structures in either open, or minimally invasive, procedures. Medtronic Navigated Reusable Instruments are specifically designed for use with the StealthStation® System, which is indicated for any medical condition in which the use of stereotactic surgery may be appropriate, and where reference to a rigid anatomical structure, such as a skull, a long bone, or vertebra can be identified relative to a CT or MR-based model, fluoroscopy images, or digitized landmarks of the anatomy. Medtronic Navigated Reusable Instruments are also compatible with the IPC® POWEREASE™ System.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K153442: CD HORIZON Spinal System, Medtronic Navigated Manual Reusable Instruments for Use with the STEALTHSTATION System, Medtronic Reusable Instruments for Use with the IPC POWEREASE System, Medtronic Navigated Reusable Instruments for Use with the STEALTHSTATION and IPC POWEREASE Systems.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K153442

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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