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FDA 510(k)

BNF

K-Number: K021782 · 2002-08-26

ApplicantAap Implantate AG
Decision Date2002-08-26
Product CodeJDS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BNF is the device name listed in this FDA 510(k) record. The listed applicant is Aap Implantate AG. It received FDA 510(k) clearance on 2002-08-26 under 510(k) number K021782. The device is classified under product code JDS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BNF?

BNF is a medical device that received FDA 510(k) clearance on 2002-08-26. The listed applicant is Aap Implantate AG. The 510(k) number is K021782.

When did BNF receive FDA 510(k) clearance?

BNF received FDA 510(k) clearance on 2002-08-26, under 510(k) number K021782.

Who is the listed applicant for BNF?

The FDA 510(k) record lists Aap Implantate AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BNF?

The FDA product code for BNF is JDS.

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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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