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FDA 510(k)

CONCORDE LIFT

K-Number: K182349 · 2019-04-03

ApplicantMedos International SARL
Decision Date2019-04-03
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CONCORDE LIFT is a medical device manufactured by Medos International SARL. It received FDA 510(k) clearance on 2019-04-03 under approval number K182349. 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 CONCORDE LIFT?

CONCORDE LIFT is a medical device that received FDA 510(k) clearance on 2019-04-03. It is manufactured by Medos International SARL. The 510(k) number is K182349.

When was CONCORDE LIFT approved by the FDA?

CONCORDE LIFT received FDA 510(k) clearance on 2019-04-03, under approval number K182349.

What company makes CONCORDE LIFT?

CONCORDE LIFT is manufactured by Medos International SARL.

What is the FDA product code for CONCORDE LIFT?

The FDA product code for CONCORDE LIFT is MAX.

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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.

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