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FDA 510(k)

ALLTHREAD PEEK ANCHOR WITH TANTALUM MARKER

K-Number: K071569 · 2007-07-02

ApplicantBiomet, Inc.
Decision Date2007-07-02
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ALLTHREAD PEEK ANCHOR WITH TANTALUM MARKER is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2007-07-02 under 510(k) number K071569. 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 ALLTHREAD PEEK ANCHOR WITH TANTALUM MARKER?

ALLTHREAD PEEK ANCHOR WITH TANTALUM MARKER is a medical device that received FDA 510(k) clearance on 2007-07-02. The listed applicant is Biomet, Inc.. The 510(k) number is K071569.

When did ALLTHREAD PEEK ANCHOR WITH TANTALUM MARKER receive FDA 510(k) clearance?

ALLTHREAD PEEK ANCHOR WITH TANTALUM MARKER received FDA 510(k) clearance on 2007-07-02, under 510(k) number K071569.

Who is the listed applicant for ALLTHREAD PEEK ANCHOR WITH TANTALUM MARKER?

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

What is the FDA product code for ALLTHREAD PEEK ANCHOR WITH TANTALUM MARKER?

The FDA product code for ALLTHREAD PEEK ANCHOR WITH TANTALUM MARKER 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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