510(k) K220843

OAKTREE Anterior Lumbar Plate and Screw System by Oak Tree Engineering, LLC — Product Code KWQ

K220843 is an FDA 510(k) premarket notification submitted by Oak Tree Engineering, LLC for the device "OAKTREE Anterior Lumbar Plate and Screw System". The FDA issued a decision of Substantially Equivalent on Dec 7, 2022. The device falls under product code KWQ (Appliance, Fixation, Spinal Intervertebral Body), a Class II device regulated under 21 CFR 888.3060. Oak Tree Engineering, LLC has 1 other 510(k) clearance on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Dec 7, 2022
Date Received
Mar 23, 2022
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Appliance, Fixation, Spinal Intervertebral Body
Device Class
Class II
Regulation Number
888.3060
Review Panel
OR
Submission Type
510(k)