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

FDA 510(k)

LP CAGE

K-Number: K110067 · 2011-04-08

ApplicantMedyssey Co, Ltd.
Decision Date2011-04-08
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LP CAGE is the device name listed in this FDA 510(k) record. The listed applicant is Medyssey Co, Ltd.. It received FDA 510(k) clearance on 2011-04-08 under 510(k) number K110067. 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 LP CAGE?

LP CAGE is a medical device that received FDA 510(k) clearance on 2011-04-08. The listed applicant is Medyssey Co, Ltd.. The 510(k) number is K110067.

When did LP CAGE receive FDA 510(k) clearance?

LP CAGE received FDA 510(k) clearance on 2011-04-08, under 510(k) number K110067.

Who is the listed applicant for LP CAGE?

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

What is the FDA product code for LP CAGE?

The FDA product code for LP CAGE is MAX.

Other records listing Medyssey Co, Ltd. 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.

K260036NeckTune™ 3D SA Cervical CageK242806Medyssey Navigation SystemK121670MEDYSSEY CANNULATED PEDICLE SCREWK121320C7 ANTERIOR CERVICAL INTERVERTEBRAL FUSION CAGEK121246MEDYSSY LT CAGE SYSTEMK110284NOVEL III SPINAL FIXATION AND ADJUSTABLE BRIDGE SYSTEM

View all 12 devices →

Related Devices (Code: MAX)

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.

K261049SCALA® TLSpineart SAK261430TruLift Expandable SystemLife Spine, Inc.K253011Catalyft PL Expandable Interbody SystemMedtronic Sofamor Danek USA, Inc.K261020Symmetrix™ L Spinal SystemMedtronic Sofamor Danek USA, Inc.K253420Admiral ACP System; Explorer TO System; Laminoplasty System; Manta Ray TDF Spacer; Meridian Interbody System; Meridian Anterior Plate System; Reef L Interbody System; Reef TO/TA System; Regatta Lateral System; Regatta Lateral Plate System; Shoreline ACS Interbody System; Shoreline Threaded TruProfile Plate; Shoreline RT Interbody System; Vu Mesh; WaveForm A Interbody System; WaveForm C Interbody System; WaveForm L Interbody System; WaveForm TA Interbody System; WaveForm TO Interbody SySeaSpine Orthopedics CorporationK253151Fule Interbody Fusion Cage SystemBeijing Fule Science & Technology Development Co., Ltd.

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.

↑