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FDA 510(k)

TRUESPAN Meniscal Repair System

K-Number: K153667 · 2016-03-24

ApplicantMedos International SARL
Decision Date2016-03-24
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TRUESPAN Meniscal Repair System is the device name listed in this FDA 510(k) record. The listed applicant is Medos International SARL. It received FDA 510(k) clearance on 2016-03-24 under 510(k) number K153667. 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 TRUESPAN Meniscal Repair System?

TRUESPAN Meniscal Repair System is a medical device that received FDA 510(k) clearance on 2016-03-24. The listed applicant is Medos International SARL. The 510(k) number is K153667.

When did TRUESPAN Meniscal Repair System receive FDA 510(k) clearance?

TRUESPAN Meniscal Repair System received FDA 510(k) clearance on 2016-03-24, under 510(k) number K153667.

Who is the listed applicant for TRUESPAN Meniscal Repair System?

The FDA 510(k) record lists Medos International SARL as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRUESPAN Meniscal Repair System?

The FDA product code for TRUESPAN Meniscal Repair System is MBI.

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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.

K262047Grappler Suture Anchor SystemParagon 28, Inc.K262369AIR+ All-Inside Meniscal Repair Device, Curved Up;AIR+ All-Inside Meniscal Repair Device, Curved DownStryker EndoscopyK261770Suture Button Repair SystemSkeletal Dynamics, Inc.K261632Thunderbolt SystemResponsive Arthroscopy, Inc.K261968Q-FIX KNOTLESS All-Suture Anchor, 2.8mm, with one black knotless and one blue MINITAPE suture (72205981); Q-FIX KNOTLESS All-Suture Anchor, 2.8mm, with one blue knotless and one black MINITAPE suture (72205982)Smith & Nephew, Inc.K260018Arthrex FiberButtonArthrex, Inc.

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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