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FDA 510(k)

IMPLASA-HOECHST GMBH IMPLANTS

K-Number: K071240 · 2008-01-24

ApplicantImplasa-Hoechst GmbH
Decision Date2008-01-24
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IMPLASA-HOECHST GMBH IMPLANTS is the device name listed in this FDA 510(k) record. The listed applicant is Implasa-Hoechst GmbH. It received FDA 510(k) clearance on 2008-01-24 under 510(k) number K071240. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPLASA-HOECHST GMBH IMPLANTS?

IMPLASA-HOECHST GMBH IMPLANTS is a medical device that received FDA 510(k) clearance on 2008-01-24. The listed applicant is Implasa-Hoechst GmbH. The 510(k) number is K071240.

When did IMPLASA-HOECHST GMBH IMPLANTS receive FDA 510(k) clearance?

IMPLASA-HOECHST GMBH IMPLANTS received FDA 510(k) clearance on 2008-01-24, under 510(k) number K071240.

Who is the listed applicant for IMPLASA-HOECHST GMBH IMPLANTS?

The FDA 510(k) record lists Implasa-Hoechst GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMPLASA-HOECHST GMBH IMPLANTS?

The FDA product code for IMPLASA-HOECHST GMBH IMPLANTS is DZE.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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