Cleared Traditional

UNiD IB3D ALIF

K200316 · Medicrea International SA · Orthopedic

Oct 2020

Decision

266d

Days

Class 2

Risk

About This 510(k) Submission

K200316 is an FDA 510(k) clearance for the UNiD IB3D ALIF, a Intervertebral Fusion Device With Bone Graft, Lumbar (Class II — Special Controls, product code MAX), submitted by Medicrea International SA (Rillieux-La-Pape, FR). The FDA issued a Cleared decision on October 30, 2020, 266 days after receiving the submission on February 7, 2020. This device falls under the Orthopedic review panel. Regulated under 21 CFR 888.3080.

Submission Details

510(k) Number	K200316 FDA.gov
FDA Decision	Cleared SESE
Date Received	February 07, 2020
Decision Date	October 30, 2020
Days to Decision	266 days
Submission Type	Traditional
Review Panel	Orthopedic (OR)
Summary	Summary PDF

Device Classification

Product Code	MAX — Intervertebral Fusion Device With Bone Graft, Lumbar
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 888.3080
Definition	Intended To Stabilize Spinal Segment To Promote Fusion In Order To Restrict Motion And Decrease Pain Using Bone Graft.