FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CrossRoads Tray System

K Number: K202268 · Decision Dec 30, 2020
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
279
Applicant Total
13
Review Days
141

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Basic Information

Device Name
CrossRoads Tray System
K Number
K202268
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Crossroads Extremity Systems, LLC
Date Received
August 11, 2020
Decision Date
December 30, 2020
Product Code
KCT
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

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K220797 FootHold System
K190658 MIS Bunion Plating System
K181872 MIS Bunion System
K181866 MotoCLIP/HiMAX Step Staple Implant System
K181410 MotoCLIP/HiMAX Implant System
K173710 MotoBAND CP Implant System
K160118 STROPP (Single Tunnel Repair of Plantar Plate)
K160300 MotoBand(TM) CP Implant System
K152306 MotoBand¿ CP Implant System
Search all 13 clearances from Crossroads Extremity Systems, LLC →