BIOMET SPORTS MEDICINE JUGGERKNOT (TM) MINI SOFT ANCHOR
K-Number: K110879 · 2011-08-19
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Device Summary
Frequently Asked Questions
What is the BIOMET SPORTS MEDICINE JUGGERKNOT (TM) MINI SOFT ANCHOR?
BIOMET SPORTS MEDICINE JUGGERKNOT (TM) MINI SOFT ANCHOR is a medical device that received FDA 510(k) clearance on 2011-08-19. The listed applicant is Biomet Sports Medicine. The 510(k) number is K110879.
When did BIOMET SPORTS MEDICINE JUGGERKNOT (TM) MINI SOFT ANCHOR receive FDA 510(k) clearance?
BIOMET SPORTS MEDICINE JUGGERKNOT (TM) MINI SOFT ANCHOR received FDA 510(k) clearance on 2011-08-19, under 510(k) number K110879.
Who is the listed applicant for BIOMET SPORTS MEDICINE JUGGERKNOT (TM) MINI SOFT ANCHOR?
The FDA 510(k) record lists Biomet Sports Medicine as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIOMET SPORTS MEDICINE JUGGERKNOT (TM) MINI SOFT ANCHOR?
The FDA product code for BIOMET SPORTS MEDICINE JUGGERKNOT (TM) MINI SOFT ANCHOR is MBI.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Biomet Sports Medicine as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: MBI)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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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