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510(k) K203327

Device
VERTACONNECT TLIF Cage
Applicant
SIGNUS Medizintechnik
510(k) number
K203327
Product code
MAX  
Decision
Substantially Equivalent (SESE)
Decision date
2021-01-25
Date received
2020-11-12
Regulation
888.3080
Classification name
Intervertebral Fusion Device With Bone Graft, Lumbar
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Antje Schmidt
Address
Industriestrasse 2 Alzenau DE 63755 63755

FDA Registration Numbers

Source Documents

510(k) summary PDF

Related GUDID Devices

Primary DIBrandCompanyPublished
04047844066744VERTACONNECT 11°SIGNUS Medizintechnik GmbH2021-03-18
04047844066737VERTACONNECT 15°SIGNUS Medizintechnik GmbH2021-03-18
04047844066720VERTACONNECT 11°SIGNUS Medizintechnik GmbH2021-03-18
04047844066713VERTACONNECT 15°SIGNUS Medizintechnik GmbH2021-03-18
04047844066706VERTACONNECT 11°SIGNUS Medizintechnik GmbH2021-03-18
04047844066690VERTACONNECT 11°SIGNUS Medizintechnik GmbH2021-03-18
04047844066683VERTACONNECT 15°SIGNUS Medizintechnik GmbH2021-03-18
04047844066676VERTACONNECT 11°SIGNUS Medizintechnik GmbH2021-03-18
04047844066669VERTACONNECT 15°SIGNUS Medizintechnik GmbH2021-03-18
04047844066652VERTACONNECT 11°SIGNUS Medizintechnik GmbH2021-03-18
04047844066645VERTACONNECT 11°SIGNUS Medizintechnik GmbH2021-03-18
04047844066638VERTACONNECT 15°SIGNUS Medizintechnik GmbH2021-03-18
04047844066621VERTACONNECT 11°SIGNUS Medizintechnik GmbH2021-03-18
04047844066614VERTACONNECT 15°SIGNUS Medizintechnik GmbH2021-03-18
04047844066607VERTACONNECT 11°SIGNUS Medizintechnik GmbH2021-03-18

Other 510(k) Records For Product Code MAX  

510(k)DeviceApplicantDecision date
K260506Ventana® P/T Lumbar Interbody SystemSpinal Elements, Inc.2026-05-15
K260837VersaLift Expandable SystemLife Spine, Inc.2026-05-12
K260385aprevo® anterior and lateral lumbar interbody system; aprevo® posterior and transforaminal lumbar interbody system; aprevo® cervical interbody system; corra™ cervical plating systemCarlsmed, Inc.2026-05-09
K261067BEE PLIF CageNGMedical GmbH2026-04-30
K254017SWINGO-3D Lumbar Cage SystemImplanet2026-02-26
K253583LUX Expandable Lumbar Interbody SystemXenix Medical2026-02-23
K250773Luna® Ti Interbody Fusion SystemSpinal Elements, Inc.2026-02-04
K253748Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer SystemLife Spine, Inc.2026-01-23
K253266Titanium Interbody SystemSpine Innovation, LLC2026-01-08
K253577IB3D™ PL Spinal System (A24000000 / IB3D Universal Implant Inserter)Medicrea International S.A.S. (Medtronic)2025-12-19
K252610ZSFab Lumbar Interbody SystemZsfab, Inc.2025-11-25
K252351UniSpace® TPLIF CageCg Medtech Co., Ltd.2025-10-28
K253377Expandable Titanium PLIF/TLIF SystemSpectrum Spine, Inc.2025-10-24
K251479Mobarn 80:20 Lumbar Interbody Fusion System (Posterior Lumbar Interbody Fusion Cage (PLIF)); Mobarn 80:20 Lumbar Interbody Fusion System (Transforaminal Lumbar Interbody Fusion Cage (TLIF)); Mobarn 80:20 Lumbar Interbody Fusion System (Direct Lateral Lumbar Interbody Fusion Cage (DLIF)); Mobarn 80:20 Lumbar Interbody Fusion System (Anterior Lumbar Interbody Fusion Cage (ALIF))Mobarn Medical Devices, LLC2025-09-18
K251444Endoskeleton™ Interbody SystemsMedtronic Sofamor Danek USA, Inc.2025-09-04

Legacy Summary

summary

FDA Review

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