Product code MRW— Unknown
FACET SCREW SYSTEM
- Classification name
- System, Facet Screw Spinal Device
- Device class
- Unclassified
- Advisory panel
- Unknown
- Total cleared
- 78
- First cleared
- Most recent
Market context for product code MRW
FDA has cleared devices under product code MRW between 1997 and 2026, filed by 46 applicant companies. No FDA device recalls reference this product code.
Clearances per year
last 15 years- 2026
- 2025
- 2024
- 2023
- 2022
- 2019
- 2018
- 2017
- 2016
- 2015
- 2013
- 2012
- 2011
- 2010
- 2009
Top applicants under product code MRW
Recent clearances under product code MRW
- K261209 — Ion-L
- K253676 — CORUS Posterior Cervical Stabilization System 3D (CORUS PCSS 3D)
- K253432 — DiversiVy Facet Screw System
- K251714 — Ion-C
- K250679 — FFX Facet Fixation System
- K253190 — CORUS-LX Implant
- K252153 — FFX Facet Fixation System
- K251885 — CAVUX Facet Fixation System (CAVUX FFS) and CORUS-LX Implant
- K250920 — Arthrex Spine Compression FT Screw
- K242527 — The Karma® Fixation System
- K243865 — AERO MIS Facet Fusion System
- K243265 — Ion 3D
- K242650 — zLOCK Lumbar Facet Fixation System
- K241035 — PMT Posterior Cervical Stabilization System (PCSS)
- K241416 — Ion 3D
- K232468 — SC Medica FFX
- K240085 — zLOCK Lumbar Facet Fixation System
- K240086 — Ion 3D
- K230840 — PMT Facet Fixation System, Lumbar (PMT FFS-LX)
- K232877 — FaSet Fixation System, UNITY Sacroiliac Joint Fixation System, Huvex Interspinous Fixation System, and AEON-C Stand Alone System
- K230297 — PMT Expandable Cage (PMT EXP)
- K220951 — PMT Facet Fixation System (PMT FFS)
- K222515 — FaSet Fixation System
- K211855 — Ion Facet Screw System
- K192744 — CORRIDOR Fixation System
- K192281 — AEGIS Anterior Lumbar Plate System, ALC Dynamized Fixation System, Anterior ISOLA Spine System, BOWTI Anterior Buttress Staple Spinal System, DISCOVERY Screw System, EXPEDIUM Anterior Spine System, FRONTIER Anterior Scoliosis System, KANEDA Anterior Scoliosis System, KANEDA SR Anterior Spinal System, M-2 Anterior Plate System, MOUNTAINEER Laminoplasty System, PROFILE Anterior Thoracolumbar Plate System, UNIVERSITY PLATE Anterior System, VIPER F2 Facet Fixation System
- K183589 — PMT Facet Screw
- K180729 — FaSet Fixation System
- K173198 — Facet Screw Fixation System
- K163374 — ALLY Facet Screws
- K161798 — FacetBRIDGE® System
- K152137 — FacetBRIDGE System
- K150223 — Facet-Link Stabilization Platform
- K142980 — Proficient (TM) Facet Screw Spine System
- K132859 — INTEGRA FACET FIXATION SYSTEM
- K132126 — SPECTRUM SPINE FENESTRATED FACET SCREW SYSTEM
- K130863 — FACET SCREW SYSTEM
- K131417 — FACET FIXX
- K120597 — KOMPREDA
- K123932 — ZYGAFIX SPINAL FACET SCREW SYSTEM
- K123497 — FACET SCREW SYSTEM
- K123218 — ILLICO FS FACET FIXATION SYSTEM
- K121551 — RESOLUTE FACET SCREW SYSTEM
- K120340 — VENUS FACET SCREW SYSTEM
- K121850 — Typhoon(TM) Facet Screw Fixation System
- K113011 — SPARTAN S3 FACET SYSTEM
- K110170 — RAPTOR FACET FIXATION SYSTEM
- K112097 — GIBRALT SPINE SYSTEMS FACET SCREW 04.0,04.5
- K101762 — VIPER F2 FACET FIXATION SYSTEM
- K101765 — KYPHON ANCHOR FACET SCREW SYSTEM
- K102438 — PRIMALOK FACET FIXATION SYSTEM
- K101364 — LANX FACET SCREW SYSTEM
- K101284 — FACET SCREW SYSTEM
- K100154 — FIXCET SPINAL FACET SCREW SYSTEM
- K092568 — SPARTAN S3 FACET SYSTEM
- K092464 — SPINEOLOGY FACET SCREW
- K090952 — ZYFUSE FACET FIXATION SYSTEM
- K090865 — LIFE SPINE FACET SCREW SPINAL SYSTEM
- K090767 — PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER
- K083442 — CORRIDOR FIXATION SYSTEM
- K082795 — SINGLE USE PERPOS PLS SYSTEM, 4.5 BONE-LOK PLS IMPLANT
- K073515 — TRANS1 FACET SCREW
- K071420 — CHAMELEON FIXATION SYSTEM
- K062391 — DISPOSABLE POSTERIOR LUMBAR STABILIZATION PROCEDURE KIT, MODELS 9045-01 AND 9045-02; COMPRESSION TOOL, MODEL 6113-00
- K061041 — US SPINE FACET FIXATION SYSTEM
- K052043 — 3.8MM CS FACET COMPRESSION DEVICE
- K051856 — TRANS1 FACET SCREWS
- K051949 — 4.5 MM LS FACET COMPRESSION DEVICE WITH POLYMER WASHER, MODEL LSPW-45-3040
- K043351 — 4.5MM BONE-LOK FACET SCREW, MODELS TFCD-45-3040S OR N; SFCD-45-3040S OR N
- K031657 — STRYKER SPINE OASYS BONE SCREW
- K021705 — MODIFICATION TO TOWNLEY TRANSFACEPEDICULAR SCREW FIXATION SYSTEM
- K020411 — NUVASIVE TRIAD FACET SCREW SYSTEM
- K013829 — MODIFICATION TO TOWNLEY TRANSFACETPEDICULAR SCREW FIXATION SYSTEM
- K012773 — DISCOVERY FACET SCREW FIXATION SYSTEM
- K003928 — TOWNLEY TRANSFACETPEDICULAR SCREW FIXATION SYSTEM
- K001323 — NUVASIVE PERCUTANEOUS TRANSFACET/INTRAPEDICULAR SCREW
- K994308 — NUVASIVE TOWNLEY FACET SCREW
- K953076 — TOWNLEY FACET/PEDICULAR SCREW PLATING SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.