510(k) K222465

Tyber Medical Anatomical Plating System by Tyber Medical, LLC — Product Code HRS

K222465 is an FDA 510(k) premarket notification submitted by Tyber Medical, LLC for the device "Tyber Medical Anatomical Plating System". The FDA issued a decision of Substantially Equivalent on March 7, 2023. The device falls under product code HRS (Plate, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Tyber Medical, LLC has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 7, 2023
Date Received
August 15, 2022
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Plate, Fixation, Bone
Device Class
Class II
Regulation Number
888.3030
Review Panel
OR
Submission Type