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FDA 510(k)

TITANIUM TOGGLE BUTTON(S)

K-Number: K033838 · 2004-02-13

ApplicantBiomet Manufacturing, Inc.
Decision Date2004-02-13
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TITANIUM TOGGLE BUTTON(S) is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Manufacturing, Inc.. It received FDA 510(k) clearance on 2004-02-13 under 510(k) number K033838. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TITANIUM TOGGLE BUTTON(S)?

TITANIUM TOGGLE BUTTON(S) is a medical device that received FDA 510(k) clearance on 2004-02-13. The listed applicant is Biomet Manufacturing, Inc.. The 510(k) number is K033838.

When did TITANIUM TOGGLE BUTTON(S) receive FDA 510(k) clearance?

TITANIUM TOGGLE BUTTON(S) received FDA 510(k) clearance on 2004-02-13, under 510(k) number K033838.

Who is the listed applicant for TITANIUM TOGGLE BUTTON(S)?

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

What is the FDA product code for TITANIUM TOGGLE BUTTON(S)?

The FDA product code for TITANIUM TOGGLE BUTTON(S) is MBI.

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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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