510(k) K210483

MOBIO Total Knee System by B-One Ortho, Corp. — Product Code JWH

K210483 is an FDA 510(k) premarket notification submitted by B-One Ortho, Corp. for the device "MOBIO Total Knee System". The FDA issued a decision of Substantially Equivalent on April 21, 2021. The device falls under product code JWH (Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer), a Class II device regulated under 21 CFR 888.3560. B-One Ortho, Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 21, 2021
Date Received
February 19, 2021
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Device Class
Class II
Regulation Number
888.3560
Review Panel
OR
Submission Type