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FDA 510(k)

AESCULAP ABC CERVICAL PLATING SYSTEM

K-Number: K974706 · 1998-03-13

ApplicantAesculap, Inc.
Decision Date1998-03-13
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

AESCULAP 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 1998-03-13 under 510(k) number K974706. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the AESCULAP ABC CERVICAL PLATING SYSTEM?

AESCULAP ABC CERVICAL PLATING SYSTEM is a medical device that received FDA 510(k) clearance on 1998-03-13. The listed applicant is Aesculap, Inc.. The 510(k) number is K974706.

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

AESCULAP ABC CERVICAL PLATING SYSTEM received FDA 510(k) clearance on 1998-03-13, under 510(k) number K974706.

Who is the listed applicant for AESCULAP 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 AESCULAP ABC CERVICAL PLATING SYSTEM?

The FDA product code for AESCULAP 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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