510(k) Report

510(k) · Cleared

Cleared

Nuvasive NVM5 System

K123307510(k) TraditionalCleared Apr 23, 2013181-day reviewClass II21 CFR 874.1820

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

Nuvasive, Inc. · PDQ Neurosurgical Nerve Locator

Cleared on Apr 23, 2013 as substantially equivalent to K112718 (Nuvasive, Inc., 2012) and 3 other predicates after a 181-day review. Its family tree reaches back 7 generations to 1984. 33 later devices descend from it.

Decided
Apr 23, 2013
Review
181 days
Class
Class II
Product code
PDQ
Recalls
None
Predicates
4

Its longest line of descent runs back 7 generations to K842956 (1984). 51 ancestors in all. 33 later devices descend from it, 2 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2012: 1 other ancestor2005: 3 other ancestors2002: 4 other ancestors2011: 1 other ancestor2006: 1 other ancestor2004: 1 other ancestor2001: 2 other ancestors1999: 3 other ancestors1997: 3 other ancestors1995: 4 other ancestors1993: 2 other ancestors2003: 1 other ancestor1998: 1 other ancestor1996: 3 other ancestors1994: 4 other ancestors1992: 3 other ancestors1990: 3 other ancestors1985: 1 other ancestor2000: 2 other ancestors1987: 1 other ancestor2014: 3 descendants cleared2015: 2 descendants cleared2017: 4 descendants cleared2019: 4 descendants cleared2022: 2 descendants cleared2016: 1 descendant cleared2024: 2 descendants cleared2025: 3 descendants cleared2023: 4 descendants cleared2018: 3 descendants cleared2026: 3 descendants cleared2021: 2 descendants clearedK842956 · Nicolet Viking · Nicolet Biomedical Instruments · 1984K971819 · Epoch 2000 Neurological Workstation · Axon Systems, Inc. · 1997K022785 · Epoch XP Neurological Workstation; Epoch XP Lite Neurological Workstation · Axon Systems, Inc. · 2002K032741 · Epochxp Neurological Workstation,Epochxp Lite Neurological Workstation · Axon Systems, Inc. · 2003K050798 · Eclipse Neurological Workstation · Axon Systems, Inc. · 2005K061113 · Orthomon · Axon Systems, Inc. · 2006K112718 · Nuvasive NVM5 System · Nuvasive, Inc. · 201219801990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 3 other ancestors2 generations back: 8 other ancestors3 generations back: 9 other ancestors4 generations back: 16 other ancestors5 generations back: 5 other ancestors7 generations back: 3 other ancestors 1 generation forward: 2 descendants2 generations forward: 3 descendants3 generations forward: 4 descendants4 generations forward: 6 descendants5 generations forward: 6 descendants6 generations forward: 5 descendants7 generations forward: 3 descendants8 generations forward: 4 descendants K112718 · Nuvasive NVM5 System · Nuvasive, Inc. · 2012K061113 · Orthomon · Axon Systems, Inc. · 2006K050798 · Eclipse Neurological Workstation · Axon Systems, Inc. · 2005K032741 · Epochxp Neurological Workstation,Epochxp Lite Neurological Workstation · Axon Systems, Inc. · 2003K022785 · Epoch XP Neurological Workstation; Epoch XP Lite Neurological Workstation · Axon Systems, Inc. · 2002K971819 · Epoch 2000 Neurological Workstation · Axon Systems, Inc. · 1997K842956 · Nicolet Viking · Nicolet Biomedical Instruments · 1984−50+5
  1. Root · 7 generations backK842956 Nicolet VikingNicolet Biomedical Instruments · 1984
  2. 6 generations backK971819 Epoch 2000 Neurological WorkstationAxon Systems, Inc. · 1997
  3. 5 generations backK022785 Epoch XP Neurological Workstation; Epoch XP Lite Neurological…Axon Systems, Inc. · 2002
  4. 4 generations backK032741 Epochxp Neurological Workstation,Epochxp Lite Neurological WorkstationAxon Systems, Inc. · 2003
  5. 3 generations backK050798 Eclipse Neurological WorkstationAxon Systems, Inc. · 2005
  6. 2 generations backK061113 OrthomonAxon Systems, Inc. · 2006
  7. 1 generation backK112718 Nuvasive NVM5 SystemNuvasive, Inc. · 2012
  8. This deviceK123307 Nuvasive NVM5 SystemNuvasive, Inc. · 2013
  9. Descendant · cites it directly · 24 of its ownK132694 Nuvasive NVM5 SystemNu Vasive, Incorporated · 2014
  10. Descendant · 2 generations on · 23 of its ownK141968 Nuvasive NVM5 SystemNuvasive, Inc. · 2014
  11. Descendant · 3 generations on · 22 of its ownK143641 NuVasive NVM5 SystemNu Vasive, Incorporated · 2015 · Recalled
  12. Descendant · 4 generations on · 13 of its ownK152942 NuVasiveNVM5 SystemNu Vasive, Incorporated · 2016
  13. Descendant · cites it directly · 9 of its ownK140400 ES2 Neuromonitoring Accessory InstrumentsStryker Corporation · 2014

Showing 5 of 33 descendants. See all descendants

Descendants cleared per year

2014: 32015: 22016: 12017: 42018: 32019: 42021: 22022: 22023: 42024: 22025: 32026: 3
2014high 4 (2017) · low 0 (2020)2026

Most influential descendants

Showing 5 of 33 · See all
  • K132694Nuvasive NVM5 SystemNu Vasive, Incorporated · 2014 · cites it directly24descendants
  • K141968Nuvasive NVM5 SystemNuvasive, Inc. · 2014 · 2 generations on23descendants
  • K143641NuVasive NVM5 SystemNu Vasive, Incorporated · 2015 · 3 generations on22descendants
  • K152942NuVasiveNVM5 SystemNu Vasive, Incorporated · 2016 · 4 generations on13descendants
  • K140400ES2 Neuromonitoring Accessory InstrumentsStryker Corporation · 2014 · cites it directly9descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K842956Nicolet VikingNicolet Biomedical Instruments1984—
−6K971819Epoch 2000 Neurological WorkstationAxon Systems, Inc.1997—
−5K022785Epoch XP Neurological Workstation; Epoch XP Lite Neurological WorkstationAxon Systems, Inc.2002—
−4K032741Epochxp Neurological Workstation,Epochxp Lite Neurological WorkstationAxon Systems, Inc.2003—
−3K050798Eclipse Neurological WorkstationAxon Systems, Inc.2005—
−2K061113OrthomonAxon Systems, Inc.2006—
−1K112718Nuvasive NVM5 SystemNuvasive, Inc.2012—
0 (this device)K123307Nuvasive NVM5 SystemNuvasive, Inc.2013—
+1K132694Nuvasive NVM5 SystemNu Vasive, Incorporated2014—
+2K141968Nuvasive NVM5 SystemNuvasive, Inc.2014—
+3K143641NuVasive NVM5 SystemNu Vasive, Incorporated20151
+4K152942NuVasiveNVM5 SystemNu Vasive, Incorporated2016—
+1K140400ES2 Neuromonitoring Accessory InstrumentsStryker Corporation2014—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198510
198710
199030
199230
199320
199440
199540
199630
199730
199810
199930
200020
200120
200240
200310
200410
200530
200610
201110
201210

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201430
201520
201610
201740
201830
201940
202120
202220
202340
202420
202530
202630
FIG. 1 — Lineage of K123307, 1984–2026Source: 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 PDQ? 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 PDQ device

  1. #1 K243636 Neuralytix iD3 System (NTX-9001)score 16.5 · 14 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
*K112718Nuvasive NVM5 System
Summary page 1
…ble 1 - Predicate Devices ________ 510O(k) Trade -or proprietary or model name Manufacturer K 112718 NVM5 Sy'stemn NuVasive, Inc. K122742 Bendini 'Spinal R…
Nuvasive, Inc.2012—
*K122742Nuvasive Bendini Spinal Rod Bending System
Cleared while this submission was under review
Summary page 1
…Trade -or proprietary or model name Manufacturer K 112718 NVM5 Sy'stemn NuVasive, Inc. K122742 Bendini 'Spinal Rod Bending System NuVasive, Inc. K050438 -StealthStation…
Nuvasive, Inc.2012—
*K050438Stealthstation System Update
Summary page 1
…5 Sy'stemn NuVasive, Inc. K122742 Bendini 'Spinal Rod Bending System NuVasive, Inc. K050438 -StealthStation Medtronic KO012448 VectorVision Trauma…
Medtronic Surgical Navigation Technologies200511
*K012448Vectorvision Trauma
Summary page 1
…Bendini 'Spinal Rod Bending System NuVasive, Inc. K050438 -StealthStation Medtronic KO012448 VectorVision Trauma BrainLAB D. Device Description NVMS System is a medical device t…
Brainlab AG2002—

Also cleared against K112718: 3 other devices →

What descends from it? (33)

See all 33

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

NumberDeviceApplicantDecidedDescendants
K132694Nuvasive NVM5 SystemNu Vasive, Incorporated201424
K140400ES2 Neuromonitoring Accessory InstrumentsStryker Corporation20149

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 29 years and passes through 3 companies; a new generation was cleared every 1.7 years on median.
  • 6 of the 51 ancestors have a recall of any class.
  • Of its descendants, K132694 (Nu Vasive, Incorporated, 2014) has gone furthest, with 24 descendants of its own.
  • 3 other devices also cite its predicate K112718.

How does its category compare?

All PDQ devices

PDQ Neurosurgical Nerve Locator: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.

FDA decisions per year · PDQ

1in 2025

2013: 52014: 72015: 32016: 32017: 22018: 42019: 42021: 22022: 22023: 12025: 12026 (partial year): 2
2007high 7 (2014) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · PDQ

182in 2019

2013: 181 days median2014: 254 days median2015: 95 days median2016: 100 days median2018: 162 days median2019: 182 days median
2007high 254 (2014) · low 95 (2015)2026

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

Recalls per year · PDQ

No recall names PDQ since 2007.

Adverse event reports per year · PDQ

2in 2025

2013: 12015: 12016: 42017: 52018: 52019: 102020: 92021: 102022: 162023: 92024: 42025: 2
2007high 16 (2022) · low 0 (2007)2025

MAUDE reports naming product code PDQ, 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
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
2013518101
2014725400
201539501
2016310004
20172—05
2018416205
20194182010
20200—09
20212—010
20222—016
20231—09
20240—04
20251—02
20262—0—

What is it indicated for?

The NVMV5® System is a medical device that is intended for intraoperative neurophysiologic monitoring during spinal surgery. The device provides information directly to the surgeon, to help assess a patient's neurophysiologic status. NVMV5 provides this information by electrically stimulating nerves via electrodes located on surgical accessories and monitoring electromyography (EMG), transcranial motor evoked potential (TcMEP) or somatosensory evoked…

Read the full statement (433 words)

The NVMV5® System is a medical device that is intended for intraoperative neurophysiologic monitoring during spinal surgery. The device provides information directly to the surgeon, to help assess a patient's neurophysiologic status. NVMV5 provides this information by electrically stimulating nerves via electrodes located on surgical accessories and monitoring electromyography (EMG), transcranial motor evoked potential (TcMEP) or somatosensory evoked potential (SSEP) responses of nerves. The System also integrates BendiniTM software used to locate spinal implant instrumentation for the placement of spinal rods.

* XLIF® (Detection) - The XLIF (Detection) function allows the surgeon to locate and evaluate spinal nerves, and is used as a nerve avoidance tool.

* Basic & Dynamic Screw Test - The Screw Test functions allow the surgeon to locate and evaluate spinal nerves by providing proximity information before, during or after bone preparation and placement of bone screws.

* Free Run EMG - The Free Run EMVG function identifies spontaneous EMVG activity of spinal nerves by continually displaying a live stream waveform of any mechanically induced myotome contractions.

* Twitch Test (Train of Four) - The Twitch Test Function allows the surgeon to assess moderate degrees of neuromuscular block in effect by evaluating muscle contraction following a train of four stimulation pulses.

* TcMEP - Transcranial stimulation techniques for motor evoked potentials are used to assess for acute dysfunction in axonal conduction of the corticospinal tract. The TcMEP function provides an adjunctive method to allow the surgeon to monitor spinal cord and motor pathway integrity during procedures with a risk of surgically induced motor injury.

* SSEP - The SSEP function allows the surgeon to assess sensory spinal cord function in surgical procedures during which the spinal cord is at risk.

* Remote Reader - The Remote Reader function provides real time remote access to the NVMV5 System for a monitoring physician outside of the operating room.

* Guidance - The Guidance function is intended as an aid for use in either open or percutaneous pedlicle cannulation procedures in the lumbar and sacral spine (Li-Si) of adult patients, and when used in conjunction with radiographic imaging and EMG, allows the surgeon to assess the angulation of system accessories relative to patient spinal anatomy for the creation of a cannulation trajectory for bone screw placement.

* Bendini - The Bendini Spinal Rod Bending function is used to locate spinal implant system instrumentation (screws, hooks) to determine their relative location to one another to generate bend instructions to shape a spinal rod. A surgeon is able to use those instructions and bend a rod using the Bendini Bender, a mechanical rod bender.

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. “K123307: Nuvasive NVM5 System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K123307

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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