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FDA 510(k)

DVO EXTENDED ARTICULATION HUMERAL HEADS

K-Number: K073331 · 2008-02-19

ApplicantDvo Extremity Solutions, LLC
Decision Date2008-02-19
Product CodeHSD
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DVO EXTENDED ARTICULATION HUMERAL HEADS is the device name listed in this FDA 510(k) record. The listed applicant is Dvo Extremity Solutions, LLC. It received FDA 510(k) clearance on 2008-02-19 under 510(k) number K073331. The device is classified under product code HSD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DVO EXTENDED ARTICULATION HUMERAL HEADS?

DVO EXTENDED ARTICULATION HUMERAL HEADS is a medical device that received FDA 510(k) clearance on 2008-02-19. The listed applicant is Dvo Extremity Solutions, LLC. The 510(k) number is K073331.

When did DVO EXTENDED ARTICULATION HUMERAL HEADS receive FDA 510(k) clearance?

DVO EXTENDED ARTICULATION HUMERAL HEADS received FDA 510(k) clearance on 2008-02-19, under 510(k) number K073331.

Who is the listed applicant for DVO EXTENDED ARTICULATION HUMERAL HEADS?

The FDA 510(k) record lists Dvo Extremity Solutions, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DVO EXTENDED ARTICULATION HUMERAL HEADS?

The FDA product code for DVO EXTENDED ARTICULATION HUMERAL HEADS is HSD.

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Other records listing Dvo Extremity Solutions, LLC as applicant

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K060988TOTAL AND HEMI SHOULDER SYSTEMK052754WRIST FUSION PLATEK052150VOLAR PLATE SYSTEM

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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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