FDA 510(k) Applications Submitted by THE ORTHOPAEDIC IMPLANT COMPANY

FDA 510(k) Number Submission Date Device Name Applicant
K160222 01/29/2016 OIC Cervical PEEK Spacer THE ORTHOPAEDIC IMPLANT COMPANY
K181184 05/03/2018 OIC Intramedullary Nail System The Orthopaedic Implant Company
K182736 09/28/2018 OIC Suture Anchor System The Orthopaedic Implant Company
K113123 10/21/2011 OIC CANNULATED SCREW SYSTEM, OIC SLIDING HIP SCREW (SHS) SYSTEM THE ORTHOPAEDIC IMPLANT COMPANY


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