510(k) Report

510(k) · Cleared

Cleared

MIS Z-Pedicle Screw System

K143200510(k) TraditionalCleared Feb 3, 201589-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

Z-Medical GmbH & Co. KG · NKB Thoracolumbosacral Pedicle Screw System

Cleared on Feb 3, 2015 as substantially equivalent to K031655 (Medtronic Sofamor Danek USA, Inc., 2003) and 2 other predicates after an 89-day review. Its family tree reaches back 14 generations to 1985. 14 later devices descend from it.

Decided
Feb 3, 2015
Review
89 days
Class
Class II
Product code
NKB
Recalls
None
Predicates
3

Its longest line of descent runs back 14 generations to K853033 (1985). 76 ancestors in all. 14 later devices descend from it, 3 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2009: 1 other ancestor2003: 5 other ancestors2012: 1 other ancestor2008: 3 other ancestors2007: 3 other ancestors2006: 4 other ancestors2004: 7 other ancestors1998: 5 other ancestors1997: 1 other ancestor1994: 1 other ancestor2005: 6 other ancestors2001: 7 other ancestors2002: 3 other ancestors2000: 3 other ancestors1999: 6 other ancestors1996: 3 other ancestors1995: 3 other ancestors2015: 1 descendant cleared2019: 1 descendant cleared2017: 2 descendants cleared2024: 3 descendants cleared2016: 1 descendant cleared2021: 1 descendant cleared2018: 2 descendants cleared2026: 1 descendant cleared2020: 1 descendant cleared2023: 1 descendant 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. · 2008K101993 · Viper System, Expedium System · Depuy Spine, Inc. · 2010 · recalledK131802 · Expedium, Viper. Viper 2 Spine System · Depuy Spine, A Johnson & Johnson Company · 20131990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 2 other ancestors2 generations back: 12 other ancestors3 generations back: 10 other ancestors4 generations back: 11 other ancestors5 generations back: 6 other ancestors6 generations back: 9 other ancestors7 generations back: 10 other ancestors8 generations back: 2 other ancestors 1 generation forward: 3 descendants2 generations forward: 3 descendants3 generations forward: 3 descendants4 generations forward: 2 descendants5 generations forward: 1 descendant6 generations forward: 1 descendant7 generations forward: 1 descendant K131802 · Expedium, Viper. Viper 2 Spine System · Depuy Spine, A Johnson & Johnson Company · 2013K101993 · Viper System, Expedium System · Depuy Spine, Inc. · 2010 · recalledK080313 · 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 backK101993 Viper System, Expedium SystemDepuy Spine, Inc. · 2010 · Recalled
  5. 1 generation backK131802 Expedium, Viper. Viper 2 Spine SystemDepuy Spine, A Johnson & Johnson Company · 2013
  6. This deviceK143200 MIS Z-Pedicle Screw SystemZ-Medical GmbH & Co. KG · 2015
  7. Descendant · cites it directly · 11 of its ownK151727 Everest Spinal SystemK2m, Inc. · 2015
  8. Descendant · 2 generations on · 9 of its ownK161369 EVEREST Spinal SystemK2m, Incorporated · 2016
  9. Descendant · 3 generations on · 6 of its ownK181188 EVEREST Spinal SystemK2m, Inc. · 2018
  10. Descendant · 4 generations on · 5 of its ownK181603 EVEREST Spinal System, RANGE (MESA and DENALI) Spinal System…K2m, Inc. · 2018
  11. Descendant · 5 generations on · 4 of its ownK222684 XIA® 4.5 Spinal System, XIA® 4.5 Cortical Trajectory, XIA® 3 Spinal…Stryker Spine · 2023
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 backK101993 Viper System, Expedium SystemDepuy Spine, Inc. · 2010 · Recalled
  14. 1 generation backK131802 Expedium, Viper. Viper 2 Spine SystemDepuy Spine, A Johnson & Johnson Company · 2013
  15. This deviceK143200 MIS Z-Pedicle Screw SystemZ-Medical GmbH & Co. KG · 2015

Showing 5 of 14 descendants. See all descendants

Descendants cleared per year

2015: 12016: 12017: 22018: 22019: 12020: 12021: 12023: 12024: 32026: 1
2015high 3 (2024) · low 0 (2022)2026

Most influential descendants

Showing 5 of 14 · See all
  • K151727Everest Spinal SystemK2m, Inc. · 2015 · cites it directly11descendants
  • K161369EVEREST Spinal SystemK2m, Incorporated · 2016 · 2 generations on9descendants
  • K181188EVEREST Spinal SystemK2m, Inc. · 2018 · 3 generations on6descendants
  • K181603EVEREST Spinal System, RANGE (MESA and DENALI) Spinal System, CASPIAN OCT (MESA Mini and…K2m, Inc. · 2018 · 4 generations on5descendants
  • K222684XIA® 4.5 Spinal System, XIA® 4.5 Cortical Trajectory, XIA® 3 Spinal System, Serrato®…Stryker Spine · 2023 · 5 generations on4descendants
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—
−2K101993Viper System, Expedium SystemDepuy Spine, Inc.20108
−1K131802Expedium, Viper. Viper 2 Spine SystemDepuy Spine, A Johnson & Johnson Company2013—
0 (this device)K143200MIS Z-Pedicle Screw SystemZ-Medical GmbH & Co. KG2015—
+1K151727Everest Spinal SystemK2m, Inc.2015—
+2K161369EVEREST Spinal SystemK2m, Incorporated2016—
+3K181188EVEREST Spinal SystemK2m, Inc.2018—
+4K181603EVEREST Spinal System, RANGE (MESA and DENALI) Spinal System, CASPIAN OCT…K2m, Inc.2018—
+5K222684XIA® 4.5 Spinal System, XIA® 4.5 Cortical Trajectory, XIA® 3 Spinal System…Stryker Spine2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
199530
199630
199710
199850
199960
200030
200170
200230
200350
200470
200560
200640
200730
200830
200910
201210

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201510
201610
201720
201820
201910
202010
202110
202310
202430
202610
FIG. 1 — Lineage of K143200, 1985–2026Source: 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 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? (3)

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
*K031655CD Horizon Spinal System
Summary page 5
…510(k) Number 510(k) Holder Predicate Device MIS Z- Pedicle Screw System CD HORIZON K031655 Medtronic Additional 510(k) Number 510(k) Holde…
Medtronic Sofamor Danek USA, Inc.20031
*K090648Viper 2 System
Summary page 5
…al 510(k) Number 510(k) Holder Predicate Device VIPER 2 K090648 DePuy Spine EXPEDIUM / VIPER K131802 DePuy Spine…
Depuy Spine, Inc.2009—
*K131802Expedium, Viper. Viper 2 Spine System
Summary page 5
…Predicate Device VIPER 2 K090648 DePuy Spine EXPEDIUM / VIPER K131802 DePuy Spine / VIPER 2 4. Description of the Device 4.1. MIS Z-Pedicle S…
Depuy Spine, A Johnson & Johnson Company2013—

Also cleared against K031655: 24 other devices →

What descends from it? (14)

See all 14

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

NumberDeviceApplicantDecidedDescendants
K151727Everest Spinal SystemK2m, Inc.201511
K192680Percusys® Plus Pedicle Screw SystemJoimax GmbH20190
K171582NEO Pedicle Screw System™Neo Medical SA20170

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 30 years and passes through 7 companies; a new generation was cleared every 1.3 years on median.
  • 4 of the 76 ancestors have a recall of any class.
  • Of its descendants, K151727 (K2m, Inc., 2015) has gone furthest, with 11 descendants of its own.
  • 24 other devices also cite its predicate K031655.

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. 2015, 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 MIS Z-Pedicle Screw System is intended to provide immobilization and stabilization of the spinal segments for posterior, non-cervical pedicle fixation in skeletally mature patients as an adjunct to fusion for the following indications:

degenerative disc disease (DDD) (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies);

spondylolisthesis (grades 3 and 4) at L5-S1

trauma (i.e., fracture or dislocation)

spinal stenosis

curvatures (i.e.,scoliosis, kyphosis, and/or lordosis)

tumor

pseudoarthrosis

failed previous fusion.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K143200: MIS Z-Pedicle Screw System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K143200

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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