FDA 510(k) Applications Submitted by Douglas Fulton

FDA 510(k) Number Submission Date Device Name Applicant
K160222 01/29/2016 OIC Cervical PEEK Spacer THE ORTHOPAEDIC IMPLANT COMPANY
K140357 02/12/2014 OIC VARIABLE ANGLE SMALL FRAGMENT LOCKING PLATE SYSTEM ORTHOPAEDIC IMPLANT COMPANY
K150655 03/13/2015 OIC Intramedullary Nail System ORTHOPAEDIC IMPLANT COMPANY
K211112 04/14/2021 OIC External Fixation System Orthopaedic Implant Company
K171211 04/25/2017 OIC External Fixation System Orthopaedic Implant Company
K181184 05/03/2018 OIC Intramedullary Nail System The Orthopaedic Implant Company
K212601 08/17/2021 DRPx Locking Distal Radius Plate System Orthopaedic Implant Company
K182736 09/28/2018 OIC Suture Anchor System The Orthopaedic Implant Company
K202971 09/30/2020 DRPx Locking Distal Radius Plate System Orthopaedic Implant Company
K223118 10/03/2022 OIC Variable Angle Small Fragment Locking Plate System Orthopaedic Implant Company
K223761 12/15/2022 OIC Intramedullary Screw System Orthopaedic Implant Company
K183682 12/28/2018 OIC External Fixation System Orthopaedic Implant Company


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