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FDA 510(k)

Velofix(tm) Interbody Fusion System

K-Number: K171749 · 2017-07-13

ApplicantU&I Corporation
Decision Date2017-07-13
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Velofix(tm) Interbody Fusion System is the device name listed in this FDA 510(k) record. The listed applicant is U&I Corporation. It received FDA 510(k) clearance on 2017-07-13 under 510(k) number K171749. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Velofix(tm) Interbody Fusion System?

Velofix(tm) Interbody Fusion System is a medical device that received FDA 510(k) clearance on 2017-07-13. The listed applicant is U&I Corporation. The 510(k) number is K171749.

When did Velofix(tm) Interbody Fusion System receive FDA 510(k) clearance?

Velofix(tm) Interbody Fusion System received FDA 510(k) clearance on 2017-07-13, under 510(k) number K171749.

Who is the listed applicant for Velofix(tm) Interbody Fusion System?

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

What is the FDA product code for Velofix(tm) Interbody Fusion System?

The FDA product code for Velofix(tm) Interbody Fusion System is ODP.

Other records listing U&I Corporation 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.

K220147Aspiron S ACP SystemK210573Velofix SA Cervical CageK183243Velofix TLIF CageK190067Velofix Interbody Fusion SystemK190053SECULOK™ ACP SystemK181824CBT Screw Fixation System

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Related Devices (Code: ODP)

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.

K2530413d Cage CervicalFims Co., Ltd.K262061Tritanium® C Anterior Cervical Cage; Tritanium® PL Cage; Tritanium® TL Curved Posterior Lumbar Cage; Aero® -C Cervical Cage System; AVS® Anchor-C Cervical Cage System; AVS® TL PEEK Spacer; AVS® PL PEEK Spacers; AVS® Navigator PEEK Spacer; AVS® AS PEEK Spacer; Monterey™ AL Interbody System; Aleutian IBF System; Cascadia Interbody System; Chesapeake Stabilization System; Sahara Stabilization System; SANTORINI™ Corpectomy Cage System; MOJAVE Interbody System; VLIFT VERTEBRAL BODY REPLACEMStryker SpineK254130C.A. Medical Interbody Fusion SystemC.A. Medical, LLCK260840BluEX Cervical Expandable Cage SystemL&K BIOMED Co., Ltd.K260850OSTEOMNI SPINAL CAGES SYSTEMOsteomni, Inc.K260549ZSFab Cervical Interbody System and ZSFab Lumbar Interbody SystemZsfab, 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.

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