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FDA 510(k)

ANTERIOR COMPACT SYSTEM

K-Number: K041469 · 2004-07-30

ApplicantX-Spine Systems
Decision Date2004-07-30
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ANTERIOR COMPACT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is X-Spine Systems. It received FDA 510(k) clearance on 2004-07-30 under 510(k) number K041469. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTERIOR COMPACT SYSTEM?

ANTERIOR COMPACT SYSTEM is a medical device that received FDA 510(k) clearance on 2004-07-30. The listed applicant is X-Spine Systems. The 510(k) number is K041469.

When did ANTERIOR COMPACT SYSTEM receive FDA 510(k) clearance?

ANTERIOR COMPACT SYSTEM received FDA 510(k) clearance on 2004-07-30, under 510(k) number K041469.

Who is the listed applicant for ANTERIOR COMPACT SYSTEM?

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

What is the FDA product code for ANTERIOR COMPACT SYSTEM?

The FDA product code for ANTERIOR COMPACT SYSTEM is KWQ.

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Related Devices (Code: KWQ)

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.

K262149corra® cervical plating systemCarlsmed, Inc.K261309Palisades™ Buttress Plate SystemBethesda Medical Devices, LLCK252776ARIES Anterior Cervical Plate SystemsZheJiang Decans Medical Devices Co., Ltd.K261112CastleLoc-P Anterior Cervical Plate SystemL&K BIOMED Co., Ltd.K260570corra™ cervical plating systemCarlsmed, Inc.K260697VyPlate™ Anterior Cervical Plate SystemVy Spine, LLC

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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