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FDA 510(k)

DOC VENTRAL CERVICAL STABILIZATION SYSTEM

K-Number: K982443 · 1998-07-29

ApplicantDepuy Motech Acromed
Decision Date1998-07-29
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DOC VENTRAL CERVICAL STABILIZATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Depuy Motech Acromed. It received FDA 510(k) clearance on 1998-07-29 under 510(k) number K982443. 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 DOC VENTRAL CERVICAL STABILIZATION SYSTEM?

DOC VENTRAL CERVICAL STABILIZATION SYSTEM is a medical device that received FDA 510(k) clearance on 1998-07-29. The listed applicant is Depuy Motech Acromed. The 510(k) number is K982443.

When did DOC VENTRAL CERVICAL STABILIZATION SYSTEM receive FDA 510(k) clearance?

DOC VENTRAL CERVICAL STABILIZATION SYSTEM received FDA 510(k) clearance on 1998-07-29, under 510(k) number K982443.

Who is the listed applicant for DOC VENTRAL CERVICAL STABILIZATION SYSTEM?

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

What is the FDA product code for DOC VENTRAL CERVICAL STABILIZATION SYSTEM?

The FDA product code for DOC VENTRAL CERVICAL STABILIZATION 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 Depuy Motech Acromed 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.

K990148STACKABLE CAGE SYSTEMK984350VSP SYSTEMK984348TIMX LOW BACK SYSTEM

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.

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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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