FDA 510(k) Applications Submitted by Orthocon Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K242050 07/12/2024 Montage Settable Bone Putty Orthocon Inc.
K243506 11/12/2024 Montage-XT Settable Bone Putty Orthocon Inc.
K243526 11/14/2024 MONTAGE Settable, Resorbable Bone Putty MONTAGE-QS Settable, Resorbable Bone Putty MONTAGE Flowable Settable, Resorbable Bone Paste MONTAGE-XT Settable, Resorbable Hemostatic Bone Putty Orthocon Inc.


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