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FDA 510(k)

AESCULAP CRANIOFACIAL TITANIUM PLATES AND SCREWS

K-Number: K923705 · 1994-02-01

ApplicantAesculap, Inc.
Decision Date1994-02-01
Product CodeJEY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

AESCULAP CRANIOFACIAL TITANIUM PLATES AND SCREWS is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 1994-02-01 under 510(k) number K923705. The device is classified under product code JEY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AESCULAP CRANIOFACIAL TITANIUM PLATES AND SCREWS?

AESCULAP CRANIOFACIAL TITANIUM PLATES AND SCREWS is a medical device that received FDA 510(k) clearance on 1994-02-01. The listed applicant is Aesculap, Inc.. The 510(k) number is K923705.

When did AESCULAP CRANIOFACIAL TITANIUM PLATES AND SCREWS receive FDA 510(k) clearance?

AESCULAP CRANIOFACIAL TITANIUM PLATES AND SCREWS received FDA 510(k) clearance on 1994-02-01, under 510(k) number K923705.

Who is the listed applicant for AESCULAP CRANIOFACIAL TITANIUM PLATES AND SCREWS?

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 CRANIOFACIAL TITANIUM PLATES AND SCREWS?

The FDA product code for AESCULAP CRANIOFACIAL TITANIUM PLATES AND SCREWS is JEY.

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Other records listing Aesculap, Inc. as applicant

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Related Devices (Code: JEY)

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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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