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FDA 510(k)

BIOMET SPORTS MEDICINE JUGGERKNOT SOFT ANCHOR

K-Number: K110145 · 2011-03-04

ApplicantBiomet, Inc.
Decision Date2011-03-04
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BIOMET SPORTS MEDICINE JUGGERKNOT SOFT ANCHOR is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2011-03-04 under 510(k) number K110145. 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 BIOMET SPORTS MEDICINE JUGGERKNOT SOFT ANCHOR?

BIOMET SPORTS MEDICINE JUGGERKNOT SOFT ANCHOR is a medical device that received FDA 510(k) clearance on 2011-03-04. The listed applicant is Biomet, Inc.. The 510(k) number is K110145.

When did BIOMET SPORTS MEDICINE JUGGERKNOT SOFT ANCHOR receive FDA 510(k) clearance?

BIOMET SPORTS MEDICINE JUGGERKNOT SOFT ANCHOR received FDA 510(k) clearance on 2011-03-04, under 510(k) number K110145.

Who is the listed applicant for BIOMET SPORTS MEDICINE JUGGERKNOT SOFT ANCHOR?

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 BIOMET SPORTS MEDICINE JUGGERKNOT SOFT ANCHOR?

The FDA product code for BIOMET SPORTS MEDICINE JUGGERKNOT SOFT ANCHOR 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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