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FDA 510(k)

ABC CERVICAL PLATING SYSTEM

K-Number: K000486 · 2000-04-14

ApplicantAesculap, Inc.
Decision Date2000-04-14
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ABC CERVICAL PLATING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2000-04-14 under 510(k) number K000486. 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 ABC CERVICAL PLATING SYSTEM?

ABC CERVICAL PLATING SYSTEM is a medical device that received FDA 510(k) clearance on 2000-04-14. The listed applicant is Aesculap, Inc.. The 510(k) number is K000486.

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

ABC CERVICAL PLATING SYSTEM received FDA 510(k) clearance on 2000-04-14, under 510(k) number K000486.

Who is the listed applicant for ABC CERVICAL PLATING SYSTEM?

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

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

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

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Other records listing Aesculap, Inc. 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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