Cleared Special

Remi Robotic Navigation System (K223070) - FDA 510(k) Clearance

Class II Orthopedic device cleared through the Special 510(k) pathway - typically does not require clinical trials.

K223070 · Fusion Robotics, LLC · Orthopedic device
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Optimized for regulatory review, auditing and printing
Oct 2022
Decision
28d
Days
Class 2
Risk

K223070 is an FDA 510(k) clearance for the Remi Robotic Navigation System. Classified as Orthopedic Stereotaxic Instrument within the OLO classification (a category covering orthopedic stereotaxic and surgical navigation instruments), Class II - Special Controls.

Submitted by Fusion Robotics, LLC (Louisville, US). The FDA issued a Cleared decision on October 28, 2022 after a review of 28 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 882.4560 - the FDA orthopedic device regulatory framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Fusion Robotics, LLC devices

Submission Details

510(k) Number K223070 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 30, 2022
Decision Date October 28, 2022
Days to Decision 28 days
Submission Type Special
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
94d faster than avg
Panel avg: 122d · This submission: 28d
Pathway characteristics
Modification to existing cleared device.

Device Classification

Product Code OLO Orthopedic Stereotaxic Instrument
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.4560
Definition Stereotaxic Guidance During Orthopedic Surgery Procedures. Indicated For Orthopedic Joint Or Spine Surgery. Neurological Stereotaxic Instruments Are Classified Under Product Code Haw.
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Orthopedic devices follow this clearance model.

Regulatory Consultant

Integrity Implants Inc. Dba Accelus
Sarah Braun

The regulatory consultant manages the 510(k) submission process on behalf of the applicant - coordinating technical documentation, predicate strategy and FDA communications. Identifying the consultant behind a submission is a key signal for competitive regulatory intelligence.

Regulatory Peers - OLO Orthopedic Stereotaxic Instrument

All 344
Devices cleared under the same product code (OLO) and FDA review panel - the closest regulatory comparables to K223070.
VERTICALE® Navigation Instruments
K223649 · Silony Medical GmbH · Dec 2022
RobPath® Total Hip Application
K220774 · Hangzhou Lancet Robotics Co., Ltd. · Dec 2022
SeaSpine 7D Navigation Instruments
K222753 · SeaSpine Orthopedics Corporation · Dec 2022
Cirq Arm System (2.0)
K222966 · Brainlab AG · Oct 2022
CUVIS-spine
K222698 · Curexo, Inc. · Oct 2022
ROSA® Knee System
K221928 · Orthosoft D/B/A Zimmer Cas · Oct 2022