510(k) K211650

The Radian MIS Bunion System by Nvision Biomedical Technologies, Inc. — Product Code HRS

K211650 is an FDA 510(k) premarket notification submitted by Nvision Biomedical Technologies, Inc. for the device "The Radian MIS Bunion System". The FDA issued a decision of Substantially Equivalent on November 24, 2021. The device falls under product code HRS (Plate, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Nvision Biomedical Technologies, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 24, 2021
Date Received
May 28, 2021
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