Home GUDID 00852776006706 CORUS PCSS 3D Implant, 5mm
Primary DI 00852776006706
Brand CORUS PCSS 3D Implant, 5mm
Company Providence Medical Technology, Inc.
Model DX-50-412
Device description Additively manufactured Stabilizers are used in conjunction with Fixation Screws as an integrated construct referred to as CORUS Posterior Cervical Stabilization System 3D (CORUS PCSS 3D).
Published 2026-09-30
Public version status New
Distribution status In Commercial Distribution
MRI safety MR Conditional
Rx true
OTC false
Sterile true
Single use true
Product Codes# Code, Name table Code Name MRW System, Facet Screw Spinal Device
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class MRW System, Facet Screw Spinal Device Unknown U
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00852776006706 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00852776006706 00852776006706 852776006706 0852776006706
GMDN Terms# Term, Definition table Term Definition Implantable cervical facet joint distractor A non-powered wedge-shaped device intended to be inserted within a cervical facet joint (spinal joint), i.e., intra-facet, for joint distraction; the distraction is intended to facilitate nerve root decompression and stabilization of the spine in the treatment of various spinal conditions. It is typically fenestrated or barbed and may incorporate a screw to expand to shape and/or to provide fixation within the joint and cervical spine stabilization. It typically includes single-use instruments (e.g., chisels, rasps) for implantation.
Regulatory Flags# DUNS number 969820245 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label false Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00852776006249 CORUS PCSS 3D-T Implant, 4mm DX-50-421 2026-10-26 00852776006713 CORUS Navigation Access System-G2LX DX-01-195 2026-10-26 00852776006744 CORUS PCSS 3D-T Implant, 5mm DX-50-422 2026-10-26 00852776006751 CORUS PCSS 3D-T LevelOne, 4mm DX-50-423 2026-10-26 00852776006614 CORUS PCSS 3D LevelOne, 4mm DX-50-413 2026-09-30 00852776006621 CORUS PCSS 3D Implant, 4mm DX-50-411 2026-09-30 00852776006690 CORUS NAVIGATION ACCESS SYSTEM-GLX DX-01-180 2025-11-03 00852776006478 CORUS-LX Implant, 4mm DX-50-407 2025-08-13 00852776006539 CORUS-LX Implant, 5mm DX-50-408 2025-08-13 00852776006546 CORUS-LX LevelOne, 4mm DX-50-409 2025-08-13 00852776006577 CAVUX Cage-LX, 5mm PD-31-206 2025-07-08 00852776006010 CAVUX Cervical Cage-T PD-31-100 PD-31-100 2015-09-02 00852776006270 CAVUX™ Cervical Cage-L 8x12x15mm 7 deg PD-31-602 PD-31-602 2016-10-14 00852776006324 CAVUX™ Cervical Cage-B 5mm PD-31-201 2016-09-26 00852776006430 CORUS™ Spinal System DX-22-100 2019-07-23 00852776006454 CORUS™ Allograft Delivery Instrument PD-10-400 2019-07-24 00852776006386 CAVUX™ Cervical Cage SE PD-31-220 2019-07-23 00852776006423 CAVUX™ Cervical Cage SB PD-31-202 2019-07-23 00852776006003 CAVUX Cervical Cage-B PD-31-200 PD-31-200 2015-09-02 00852776006089 DTRAX® Spinal System DX-22-100 DX-22-100 2017-06-27
Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 00852776006249 CORUS PCSS 3D-T Implant, 4mm Providence Medical Technology, Inc. MRW 2026-10-26 00852776006744 CORUS PCSS 3D-T Implant, 5mm Providence Medical Technology, Inc. MRW 2026-10-26 00852776006751 CORUS PCSS 3D-T LevelOne, 4mm Providence Medical Technology, Inc. MRW 2026-10-26 00888867614543 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614550 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614567 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614574 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614581 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614598 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614604 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614611 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614628 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614635 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614642 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614659 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614666 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614673 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614680 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614697 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614703 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614710 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614727 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614734 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614741 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614758 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614765 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614772 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614789 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614796 Arthrex® ARTHREX, INC. MRW 2026-10-07 00888867614802 Arthrex® ARTHREX, INC. MRW 2026-10-07