FDA 510(k) Applications Submitted by Mark Wylie

FDA 510(k) Number Submission Date Device Name Applicant
K234009 12/19/2023 Acorn 3D Software (AC-SEG-4009); Acorn 3DP Model (AC-101-XX) Mighty Oak Medical
K220132 01/18/2022 FIREFLY« Cervical Navigation Guide Mighty Oak Medical Inc.
K181399 05/29/2018 FIREFLY« Pedicle Screw Navigation Guide Mighty Oak Medical Inc.
K181883 07/13/2018 FIREFLY« Midline Navigation Guide Mighty Oak Medical Inc.
K162419 08/30/2016 FIREFLY« Pedicle Screw Navigation Guide MIGHTY OAK MEDICAL INC.


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