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FDA 510(k)

STEELEX STERNUM SET

K-Number: K023411 · 2002-12-19

ApplicantAesculap, Inc.
Decision Date2002-12-19
Product CodeGAQ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STEELEX STERNUM SET is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2002-12-19 under 510(k) number K023411. The device is classified under product code GAQ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STEELEX STERNUM SET?

STEELEX STERNUM SET is a medical device that received FDA 510(k) clearance on 2002-12-19. The listed applicant is Aesculap, Inc.. The 510(k) number is K023411.

When did STEELEX STERNUM SET receive FDA 510(k) clearance?

STEELEX STERNUM SET received FDA 510(k) clearance on 2002-12-19, under 510(k) number K023411.

Who is the listed applicant for STEELEX STERNUM SET?

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 STEELEX STERNUM SET?

The FDA product code for STEELEX STERNUM SET is GAQ.

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Other records listing Aesculap, Inc. as applicant

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Related Devices (Code: GAQ)

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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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