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FDA 510(k)

MAC MALE ADAPTER

K-Number: K102843 · 2011-05-03

ApplicantBiomet Trauma (Aka Ebi, LLC)
Decision Date2011-05-03
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MAC MALE ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Trauma (Aka Ebi, LLC). It received FDA 510(k) clearance on 2011-05-03 under 510(k) number K102843. 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 MAC MALE ADAPTER?

MAC MALE ADAPTER is a medical device that received FDA 510(k) clearance on 2011-05-03. The listed applicant is Biomet Trauma (Aka Ebi, LLC). The 510(k) number is K102843.

When did MAC MALE ADAPTER receive FDA 510(k) clearance?

MAC MALE ADAPTER received FDA 510(k) clearance on 2011-05-03, under 510(k) number K102843.

Who is the listed applicant for MAC MALE ADAPTER?

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

What is the FDA product code for MAC MALE ADAPTER?

The FDA product code for MAC MALE ADAPTER is KTT.

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Related Devices (Code: KTT)

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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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