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Data / Medical devices / United States / Crossroads Extremity Systems LLC

Crossroads Extremity Systems LLC: FDA-registered device maker in Memphis, TN, United States, 22 510(k) clearances

Crossroads Extremity Systems LLC is registered with the FDA (registration 3020584246) in Memphis, TN, United States. It lists 25 device types. The FDA files 22 510(k) clearances under its listings, the newest dated January 6, 2026. 2 recall events name it as the recalling firm. Registered through 2027. FDA data exported November 2, 2026.

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Get makers like this oneWatch Crossroads Extremity Systems LLC
FDA registration number
3020584246
Address
6423 Shelby View Dr Suite 101, Memphis, TN, United States, 38134
Owner or operator
CrossRoads Extremity Systems LLC (10048591)
Roles
Complaint file establishment, Manufacturer
First device listed
January 29, 2015
Registered through
2027
Brand names listed
Allograft Template, Broach, CrossCLIP Implant System, CrossRoads Bone Screw, CrossRoads Modular Tray System, CrossRoads Screw System, CrossRoads Tray System, CrossTIE and more

Devices it lists

DeviceProduct codeClassRoleSource
BenderHXW1Complaint file establishmentaccessdata.fda.gov
Bit, DrillHTW1Manufactureraccessdata.fda.gov
BroachHTQ1Manufactureraccessdata.fda.gov
CountersinkHWW1Complaint file establishmentaccessdata.fda.gov
Driver, ProsthesisHWR1Manufactureraccessdata.fda.gov
ExtractorHWB1Manufactureraccessdata.fda.gov
Fastener, Fixation, Nondegradable, Soft TissueMBI2Complaint file establishment, Manufactureraccessdata.fda.gov
Gauge, DepthHTJ1Manufactureraccessdata.fda.gov
Guide, Surgical, InstrumentFZX1Manufactureraccessdata.fda.gov
Holder, Needle; OrthopedicHXK1Complaint file establishmentaccessdata.fda.gov
Instrument, Bending Or ContouringHXP1Manufactureraccessdata.fda.gov
Orthopedic Manual Surgical InstrumentLXH1Manufactureraccessdata.fda.gov
Osteotome, ManualGFI1Complaint file establishmentaccessdata.fda.gov
PasserHWQ1Complaint file establishmentaccessdata.fda.gov
Plate, Fixation, BoneHRS2Complaint file establishment, Manufactureraccessdata.fda.gov
ProbeHXB1Complaint file establishmentaccessdata.fda.gov
ReamerHTO1Manufactureraccessdata.fda.gov
RetractorGAD1Complaint file establishmentaccessdata.fda.gov
Screw, Fixation, BoneHWC2Complaint file establishment, Manufactureraccessdata.fda.gov
ScrewdriverHXX1Complaint file establishment, Manufactureraccessdata.fda.gov
Staple, Fixation, BoneJDR2Manufactureraccessdata.fda.gov
Sterilization Wrap Containers, Trays, Cassettes & Other AccessoriesKCT2Manufactureraccessdata.fda.gov
TampHXG1Manufactureraccessdata.fda.gov
Tap, BoneHWX1Manufactureraccessdata.fda.gov
TemplateHWT1Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
January 6, 2026K253178TRILEAP Plating SystemHRSSubstantially EquivalentCrossroads Extremity Systemsaccessdata.fda.gov
July 16, 2024K241050CrossRoads Modular Tray SystemKCTSubstantially EquivalentCrossroads Extremity Systemsaccessdata.fda.gov
September 29, 2023K230591TriLEAP Plating SystemHRSSubstantially EquivalentCrossroads Extremity Systemsaccessdata.fda.gov
March 30, 2023K223342MotoBAND™ CP Implant System: DynaBunion™ 4D Minimal-incision Bunion System, DynaMET™ Lesser TMT Fusion SystemHRSSubstantially EquivalentCrossroads Extremity Systems, LLCaccessdata.fda.gov
April 15, 2022K220797FootHold SystemMBISubstantially EquivalentCrossroads Extremity Systems, LLCaccessdata.fda.gov
December 30, 2020K202268CrossRoads Tray SystemKCTSubstantially EquivalentCrossroads Extremity Systems, LLCaccessdata.fda.gov
January 10, 2020K193452MotoBAND CP Implant SystemHRSSubstantially EquivalentCrossroads Extemity Systems, LLCaccessdata.fda.gov
August 19, 2019K191342CrossRoads Screw SystemHWCSubstantially EquivalentCrossroads Extemity Systems, LLCaccessdata.fda.gov
August 16, 2019K190722TriMAX Implant SystemJDRSubstantially EquivalentCrossroads Extemity Systems, LLCaccessdata.fda.gov
April 12, 2019K190658MIS Bunion Plating SystemHRSSubstantially EquivalentCrossroads Extremity Systems, LLCaccessdata.fda.gov
August 9, 2018K181866MotoCLIP/HiMAX Step Staple Implant SystemJDRSubstantially EquivalentCrossroads Extremity Systems, LLCaccessdata.fda.gov
June 29, 2018K181410MotoCLIP/HiMAX Implant SystemJDRSubstantially EquivalentCrossroads Extremity Systems, LLCaccessdata.fda.gov
February 12, 2018K173710MotoBAND CP Implant SystemHWCSubstantially EquivalentCrossroads Extremity Systems, LLCaccessdata.fda.gov
May 5, 2016K153585Flip Button Suture AnchorMBISubstantially EquivalentFirst Ray, LLCaccessdata.fda.gov
May 3, 2016K160118STROPP (Single Tunnel Repair of Plantar Plate)MBISubstantially EquivalentCrossroads Extremity Systems, LLCaccessdata.fda.gov
April 22, 2016K160300MotoBand(TM) CP Implant SystemHRSSubstantially EquivalentCrossroads Extremity Systems, LLCaccessdata.fda.gov
December 11, 2015K152306MotoBand¿ CP Implant SystemHRSSubstantially EquivalentCrossroads Extremity Systems, LLCaccessdata.fda.gov
September 23, 2015K152072CrossRoads Screw SystemHWCSubstantially EquivalentCrossroads Extremity Systems, LLCaccessdata.fda.gov
September 4, 2015K151270CrossTIE Intraosseous Fixation SystemHWCSubstantially EquivalentCrossroads Extremity Systems, LLCaccessdata.fda.gov
January 16, 2015K143039CrossRoads Screw SystemHWCSubstantially EquivalentOrthodiscovery Group, LLC (D.B.A. Crossroads Extremaccessdata.fda.gov
January 8, 2015K141857CrossTie Intraosseous Fixation SystemHWCSubstantially EquivalentOrthodiscovery Group, LLC (D.B.A. Crossroads Extremaccessdata.fda.gov
October 24, 2014K142727CrossCLIP Implant SystemJDRSubstantially EquivalentOrthodiscovery Group, LLC(D.B.A. Crossroads Extremity Systemsaccessdata.fda.gov

Recalls

Recall events where this establishment is the recalling firm, matched on its FEI.

InitiatedEventClassStatusProductReasonSource
September 19, 201983934Class IITerminatedMotoBand CP, Poly-axial Locking Screw, 3.0mm x 28mmPotentially includes a 3.0mm x 30mm screw instead of 3.0mm x 28mm screw.accessdata.fda.gov
February 16, 201776687Class IITerminatedMotoCLIP(TM) Super Elastic Fusion System, Size 18mm x 14mm x 14mm, REF 1442-1814, Rx Only, STERILE R.Seven 18mm x 18mm x 18 mm implants had been placed in kits, packed and labeled as 18mm x 14mm x 14mm.accessdata.fda.gov

Compare with other makers

Updated January 6, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.