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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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