LOSPA IS TLIF & DLIF Cages
K-Number: K170243 · 2017-03-31
ApplicantCorentec Co., Ltd.
Decision Date2017-03-31
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
LOSPA IS TLIF & DLIF Cages is a medical device manufactured by Corentec Co., Ltd.. It received FDA 510(k) clearance on 2017-03-31 under approval number K170243. 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 LOSPA IS TLIF & DLIF Cages?
LOSPA IS TLIF & DLIF Cages is a medical device that received FDA 510(k) clearance on 2017-03-31. It is manufactured by Corentec Co., Ltd.. The 510(k) number is K170243.
When was LOSPA IS TLIF & DLIF Cages approved by the FDA?
LOSPA IS TLIF & DLIF Cages received FDA 510(k) clearance on 2017-03-31, under approval number K170243.
What company makes LOSPA IS TLIF & DLIF Cages?
LOSPA IS TLIF & DLIF Cages is manufactured by Corentec Co., Ltd..
What is the FDA product code for LOSPA IS TLIF & DLIF Cages?
The FDA product code for LOSPA IS TLIF & DLIF Cages is MAX.
Other Devices by Corentec Co., Ltd.
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.