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FDA 510(k)

RELIANCE BUTTRESS WASHER SYSTEM

K-Number: K073349 · 2008-02-13

ApplicantReliance Medical Systems, LLC
Decision Date2008-02-13
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

RELIANCE BUTTRESS WASHER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Reliance Medical Systems, LLC. It received FDA 510(k) clearance on 2008-02-13 under 510(k) number K073349. 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 RELIANCE BUTTRESS WASHER SYSTEM?

RELIANCE BUTTRESS WASHER SYSTEM is a medical device that received FDA 510(k) clearance on 2008-02-13. The listed applicant is Reliance Medical Systems, LLC. The 510(k) number is K073349.

When did RELIANCE BUTTRESS WASHER SYSTEM receive FDA 510(k) clearance?

RELIANCE BUTTRESS WASHER SYSTEM received FDA 510(k) clearance on 2008-02-13, under 510(k) number K073349.

Who is the listed applicant for RELIANCE BUTTRESS WASHER SYSTEM?

The FDA 510(k) record lists Reliance Medical Systems, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RELIANCE BUTTRESS WASHER SYSTEM?

The FDA product code for RELIANCE BUTTRESS WASHER SYSTEM is KWQ.

Related Clinical Trials

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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Other records listing Reliance Medical Systems, LLC 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.

K202266Reliance Cervical IBF SystemK210874Reliance Spinal Screw SystemK183049Reliance Lumbar IBF SystemK173283Reliance Lumbar IBF SystemK173102Reliance Cervical IBF SystemK172489Reliance Cervical IBF System

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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

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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