CAPRI Corpectomy Cage System
K-Number: K171704 · 2017-08-31
ApplicantK2m
Decision Date2017-08-31
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
CAPRI Corpectomy Cage System is a medical device manufactured by K2m. It received FDA 510(k) clearance on 2017-08-31 under approval number K171704. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the CAPRI Corpectomy Cage System?
CAPRI Corpectomy Cage System is a medical device that received FDA 510(k) clearance on 2017-08-31. It is manufactured by K2m. The 510(k) number is K171704.
When was CAPRI Corpectomy Cage System approved by the FDA?
CAPRI Corpectomy Cage System received FDA 510(k) clearance on 2017-08-31, under approval number K171704.
What company makes CAPRI Corpectomy Cage System?
CAPRI Corpectomy Cage System is manufactured by K2m.
What is the FDA product code for CAPRI Corpectomy Cage System?
The FDA product code for CAPRI Corpectomy Cage System is MQP.
Other Devices by K2m
Related Devices (Code: MQP)
K172330Blustone Synergy Silica SystemBlustone Synergy
K173125T2 STRATOSPHERE Expandable Corpectomy SystemMedtronic Sofamor Danek
K162315FORTIFY Corpectomy SpacersGlobus Medical, Inc.
K172323Omnia Medical VBROmnia Medical, LLC
K171686Choice Spine Hawkeye Vertebral Body Replacement (VBR) SystemChoicespine
K162133VerteFIT Corpectomy Cage SystemLdr Spine USA, 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.