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FDA 510(k)

DIFUSION TECHNOLOGIES XIPHOS INTERBODY FUSION SYSTEM

K-Number: K100042 · 2010-10-01

ApplicantDifusion Technologies
Decision Date2010-10-01
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DIFUSION TECHNOLOGIES XIPHOS INTERBODY FUSION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Difusion Technologies. It received FDA 510(k) clearance on 2010-10-01 under 510(k) number K100042. 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 DIFUSION TECHNOLOGIES XIPHOS INTERBODY FUSION SYSTEM?

DIFUSION TECHNOLOGIES XIPHOS INTERBODY FUSION SYSTEM is a medical device that received FDA 510(k) clearance on 2010-10-01. The listed applicant is Difusion Technologies. The 510(k) number is K100042.

When did DIFUSION TECHNOLOGIES XIPHOS INTERBODY FUSION SYSTEM receive FDA 510(k) clearance?

DIFUSION TECHNOLOGIES XIPHOS INTERBODY FUSION SYSTEM received FDA 510(k) clearance on 2010-10-01, under 510(k) number K100042.

Who is the listed applicant for DIFUSION TECHNOLOGIES XIPHOS INTERBODY FUSION SYSTEM?

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

What is the FDA product code for DIFUSION TECHNOLOGIES XIPHOS INTERBODY FUSION SYSTEM?

The FDA product code for DIFUSION TECHNOLOGIES XIPHOS INTERBODY FUSION SYSTEM is MAX.

Related Clinical Trials

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Other records listing Difusion Technologies 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.

K190544XIHPOS™ ZFUZE™ Interbody Fusion SystemK123969XIPHOS

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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