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FDA 510(k)

ANTERIOR CERVICAL PLATING SYSTEM

K-Number: K984342 · 1998-12-30

ApplicantUnited States Surgical, A Division of Tyco Healthc
Decision Date1998-12-30
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ANTERIOR CERVICAL PLATING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is United States Surgical, A Division of Tyco Healthc. It received FDA 510(k) clearance on 1998-12-30 under 510(k) number K984342. 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 CERVICAL PLATING SYSTEM?

ANTERIOR CERVICAL PLATING SYSTEM is a medical device that received FDA 510(k) clearance on 1998-12-30. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K984342.

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

ANTERIOR CERVICAL PLATING SYSTEM received FDA 510(k) clearance on 1998-12-30, under 510(k) number K984342.

Who is the listed applicant for ANTERIOR CERVICAL PLATING SYSTEM?

The FDA 510(k) record lists United States Surgical, A Division of Tyco Healthc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANTERIOR CERVICAL PLATING SYSTEM?

The FDA product code for ANTERIOR CERVICAL PLATING SYSTEM is KWQ.

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Other records listing United States Surgical, A Division of Tyco Healthc as applicant

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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.

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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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