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FDA 510(k)

MDPO FRAME SYSTEM

K-Number: K093753 · 2010-08-26

ApplicantMdpo, LLC
Decision Date2010-08-26
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MDPO FRAME SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Mdpo, LLC. It received FDA 510(k) clearance on 2010-08-26 under 510(k) number K093753. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MDPO FRAME SYSTEM?

MDPO FRAME SYSTEM is a medical device that received FDA 510(k) clearance on 2010-08-26. The listed applicant is Mdpo, LLC. The 510(k) number is K093753.

When did MDPO FRAME SYSTEM receive FDA 510(k) clearance?

MDPO FRAME SYSTEM received FDA 510(k) clearance on 2010-08-26, under 510(k) number K093753.

Who is the listed applicant for MDPO FRAME SYSTEM?

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

What is the FDA product code for MDPO FRAME SYSTEM?

The FDA product code for MDPO FRAME SYSTEM is KTT.

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Related Devices (Code: KTT)

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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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