Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CONDUIT Instruments

K-Number: K210728 · 2021-05-06

ApplicantMedos International SARL
Decision Date2021-05-06
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CONDUIT Instruments is a medical device manufactured by Medos International SARL. It received FDA 510(k) clearance on 2021-05-06 under approval number K210728. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONDUIT Instruments?

CONDUIT Instruments is a medical device that received FDA 510(k) clearance on 2021-05-06. It is manufactured by Medos International SARL. The 510(k) number is K210728.

When was CONDUIT Instruments approved by the FDA?

CONDUIT Instruments received FDA 510(k) clearance on 2021-05-06, under approval number K210728.

What company makes CONDUIT Instruments?

CONDUIT Instruments is manufactured by Medos International SARL.

What is the FDA product code for CONDUIT Instruments?

The FDA product code for CONDUIT Instruments is MAX.

Other Devices by Medos International SARL

K162247PERMATAPE K162327COUGAR® LS Lateral Cage System and COUGAR® System K162912VIPER PRIME™ additions to the VIPER® System K163106CODMAN Integrated Bipolar Cord and Tubing Set K161638SPEEDTRAP Graft Preparation System K162469CODMAN VersaTru Standard Disposable Non-Stick Bipolar Forceps, CODMAN VersaTru Slim Disposable Non-Stick Bipolar Forceps

View all 73 devices →

Related Devices (Code: MAX)

K163180Hubble IIOrbbo Surgical, LLC K162446FORZA Spacer System, PILLAR PEEK Spacer System, PILLAR SA PEEK Spacer System, SKYHAWK Lateral Interbody Fusion SystemOrthofix, Inc. K162327COUGAR® LS Lateral Cage System and COUGAR® SystemMedos International SARL K162103Choice Spine Lumbar Spacer System (Sabre™, Shark™, Hornet™, Harpoon™), Choice Spine Interbody Fusion System (Harrier™), Choice Spine Vertebral Body Replacement System (Hawkeye™)Choicespine, LP K162431Luna 3D Interbody Fusion SystemBenvenue Medical, Inc. K160959Xsert Lumbar Expandable Interbody SystemX-Spine Systems, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑