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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is K2m. It received FDA 510(k) clearance on 2017-08-31 under 510(k) 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. The listed applicant is K2m. The 510(k) number is K171704.

When did CAPRI Corpectomy Cage System receive FDA 510(k) clearance?

CAPRI Corpectomy Cage System received FDA 510(k) clearance on 2017-08-31, under 510(k) number K171704.

Who is the listed applicant for CAPRI Corpectomy Cage System?

The FDA 510(k) record lists K2m as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAPRI Corpectomy Cage System?

The FDA product code for CAPRI Corpectomy Cage System is MQP.

Other records listing K2m as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: MQP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261810Vertiwedge® Intraosseous SystemFoundation Surgical GroupK261031POSEIDON STSignus Medinzintechnik GmbHK253158VyBrate™ VBR SystemVy Spine, LLCK241468Vertiwedge® Intraosseous SystemFoundation Surgical Group, Inc.K232790KONG®-TL VBR System and KONG® C VBR SystemIcotec AGK233359DOMINION Expandable Corpectomy SystemAstura Medical

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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