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FDA 510(k)

MONDEAL EXTREMITY BONE FIXATION SYSTEM

K-Number: K072740 · 2007-11-19

Decision Date2007-11-19
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MONDEAL EXTREMITY BONE FIXATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Mondeal Medical Systems GmbH. It received FDA 510(k) clearance on 2007-11-19 under 510(k) number K072740. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONDEAL EXTREMITY BONE FIXATION SYSTEM?

MONDEAL EXTREMITY BONE FIXATION SYSTEM is a medical device that received FDA 510(k) clearance on 2007-11-19. The listed applicant is Mondeal Medical Systems GmbH. The 510(k) number is K072740.

When did MONDEAL EXTREMITY BONE FIXATION SYSTEM receive FDA 510(k) clearance?

MONDEAL EXTREMITY BONE FIXATION SYSTEM received FDA 510(k) clearance on 2007-11-19, under 510(k) number K072740.

Who is the listed applicant for MONDEAL EXTREMITY BONE FIXATION SYSTEM?

The FDA 510(k) record lists Mondeal Medical Systems GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MONDEAL EXTREMITY BONE FIXATION SYSTEM?

The FDA product code for MONDEAL EXTREMITY BONE FIXATION SYSTEM is HRS.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Mondeal Medical Systems GmbH as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: HRS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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