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FDA 510(k)

AESCULAP STERNUMFIX STERNAL CLOSURE SYSTEM

K-Number: K063017 · 2006-12-27

ApplicantAesculap, Inc.
Decision Date2006-12-27
Product CodeJDQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AESCULAP STERNUMFIX STERNAL CLOSURE 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 2006-12-27 under 510(k) number K063017. The device is classified under product code JDQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AESCULAP STERNUMFIX STERNAL CLOSURE SYSTEM?

AESCULAP STERNUMFIX STERNAL CLOSURE SYSTEM is a medical device that received FDA 510(k) clearance on 2006-12-27. The listed applicant is Aesculap, Inc.. The 510(k) number is K063017.

When did AESCULAP STERNUMFIX STERNAL CLOSURE SYSTEM receive FDA 510(k) clearance?

AESCULAP STERNUMFIX STERNAL CLOSURE SYSTEM received FDA 510(k) clearance on 2006-12-27, under 510(k) number K063017.

Who is the listed applicant for AESCULAP STERNUMFIX STERNAL CLOSURE 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 STERNUMFIX STERNAL CLOSURE SYSTEM?

The FDA product code for AESCULAP STERNUMFIX STERNAL CLOSURE SYSTEM is JDQ.

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Other records listing Aesculap, Inc. as applicant

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Related Devices (Code: JDQ)

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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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