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FDA 510(k)

AESCULAP TITANIUM BONE PLATES

K-Number: K913730 · 1992-03-12

ApplicantAesculap, Inc.
Decision Date1992-03-12
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AESCULAP TITANIUM BONE PLATES is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 1992-03-12 under 510(k) number K913730. 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 AESCULAP TITANIUM BONE PLATES?

AESCULAP TITANIUM BONE PLATES is a medical device that received FDA 510(k) clearance on 1992-03-12. The listed applicant is Aesculap, Inc.. The 510(k) number is K913730.

When did AESCULAP TITANIUM BONE PLATES receive FDA 510(k) clearance?

AESCULAP TITANIUM BONE PLATES received FDA 510(k) clearance on 1992-03-12, under 510(k) number K913730.

Who is the listed applicant for AESCULAP TITANIUM BONE PLATES?

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 TITANIUM BONE PLATES?

The FDA product code for AESCULAP TITANIUM BONE PLATES is KWQ.

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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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