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FDA 510(k)

TOP CERVICAL SPINE PLATES & TITANIUM BONE SCREWS

K-Number: K914362 · 1992-04-29

ApplicantAcorn Group, Inc.
Decision Date1992-04-29
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TOP CERVICAL SPINE PLATES & TITANIUM BONE SCREWS is the device name listed in this FDA 510(k) record. The listed applicant is Acorn Group, Inc.. It received FDA 510(k) clearance on 1992-04-29 under 510(k) number K914362. 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 TOP CERVICAL SPINE PLATES & TITANIUM BONE SCREWS?

TOP CERVICAL SPINE PLATES & TITANIUM BONE SCREWS is a medical device that received FDA 510(k) clearance on 1992-04-29. The listed applicant is Acorn Group, Inc.. The 510(k) number is K914362.

When did TOP CERVICAL SPINE PLATES & TITANIUM BONE SCREWS receive FDA 510(k) clearance?

TOP CERVICAL SPINE PLATES & TITANIUM BONE SCREWS received FDA 510(k) clearance on 1992-04-29, under 510(k) number K914362.

Who is the listed applicant for TOP CERVICAL SPINE PLATES & TITANIUM BONE SCREWS?

The FDA 510(k) record lists Acorn Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TOP CERVICAL SPINE PLATES & TITANIUM BONE SCREWS?

The FDA product code for TOP CERVICAL SPINE PLATES & TITANIUM BONE SCREWS 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 Acorn Group, Inc. 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.

K912905LARYNGOSCOPEK904126VISIRASERK900430IRRIGATION AND SUCTION APPARATUS

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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