FDA 510(k) Applications Submitted by Stryker Craniomaxillofacial (CMF)

FDA 510(k) Number Submission Date Device Name Applicant
K222650 09/01/2022 Stryker Cutomized Mandible Recon Plate; Stryker Surgeon iD Mandible Recon Plate Stryker Craniomaxillofacial (CMF)


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