Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

PDQ — Predicate Candidate Screening

36 FDA 510(k) clearances under this product code; the 50 most recent screened below.

168 daysmedian FDA review time
274 days90th percentile
36clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K260992iD3 Nav Decompression Probe (NTX-9005); iD3 Ball Tip Stim PrNeuralytix2026-06-25910
K253580Sterile Insulated Dilators, 5, 10, 16mm (MDT-0442S); SterileTedan Surgical Innovations2026-04-261600
K243636Neuralytix iD3 System (NTX-9001)Neuralytix, LLC2025-06-262130
K223438TELIGEN System Peripheral Motor Nerve Stimulation IndicationMedos International SARL2023-02-10880
K221821ATEC IOM Accessory InstrumentsAlphatec Spine, Inc.2022-09-23920
K220160PediGuard ThreadedSpineguard S.A.2022-03-31710
K203684Neurosign V4 Intraoperative Nerve MonitorMagstim Company, Ltd.2021-03-17900
K201454DSG Connect TechnologySpineguard S.A.2021-02-102540
K191723ATEC IOM Accessory InstrumentsAlphatec Spine, Inc.2019-10-181130
K190163ALARA Neuro Access KitSurGenTec, LLC2019-07-161660
K182617ATEC IOM Accessory InstrumentsAlphatec Spine, Inc.2019-05-092270
K182662NAV PAK Needle, NIM NAV PAK NeedleBoston Endo Surgical Tech,2019-04-101970
K181559Neurosign V4 Intraoperative Nerve MonitorMagstim Company, Ltd.2018-11-091490
K180542NIM PAK Needle; NIM XPAK Needle; NIM Pedicle ProbeBoston Endo Surgical Tech,2018-08-221740
K173526SENTIO MMG Gen 2Medos International SARL2018-04-051420
K173134SENTIO MMG Pedicle Access NeedlesMedos International SARL2018-03-221740
K171807ES2 Neuromonitoring Accessory InstrumentsStryker Corporation2017-07-18290
K162313NuVasive Next Generation NVM5 SystemNu Vasive, Incorporated2017-03-162100
K161893Neuromonitoring KitSI-BONE, Inc.2016-10-18990
K152747DSG Threaded Drill SystemSpineguard S.A.2016-06-102610
K152942NuVasiveNVM5 SystemNu Vasive, Incorporated2016-01-131000
K143641NuVasive NVM5 SystemNu Vasive, Incorporated2015-03-27950
K142438Nerve Monitoring Cable SystemPioneer Surgical Technology, Inc. (Rti Surgical, Inc.)2015-03-051880
K143159Cannulated PediGuard Needle#1, Cannulated PediGuard Needle#2Spineguard S.A.2015-01-23810
K141968NUVASIVE NVM5 SYSTEMNuvasive, Inc.2014-11-141160
K140088PHANTOM XL INSULATED DILATORSTedan Surgical Innovations, LLC2014-09-252540
K131304SENTIO MMGInnovative Surgical Solutions, LLC ("Iss")2014-05-293870
K132694NUVASIVE NVM5 SYSTEMNu Vasive, Incorporated2014-05-162600
K133530NUVASIVE EMG ENDOTRACHEAL TUBENu Vasive, Incorporated2014-05-021680
K132138RHYTHMLINK DISPOSABLE CONCENTRIC STIMULATING PROBERhythmlink International, LLC2014-04-112740
K132373BIOMET ACCESS SYSTEMBiomet Spine (Aka Ebi, LLC)2014-03-272400
K123390PEDIGUARD NERVE DETECTOR SYSTEMSpineguard S.A.2013-08-082790
K130806NEUROVISION INK PRINTED ENDOTRACHEAL TUBE ELECTRODENeurovision Medical Products, Inc.2013-07-121090
K120590DILATOR TUBE SETKoros USA, Inc.2013-05-074340
K123307NUVASIVE NVM5 SYSTEMNuvasive, Inc.2013-04-231810
K123589CADWELL DISPOSABLE PROBE HANDLECadwell2013-03-191180

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda