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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 a medical device manufactured by Medos International SARL. It received FDA 510(k) clearance on 2016-03-24 under approval 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. It is manufactured by Medos International SARL. The 510(k) number is K153667.

When was TRUESPAN Meniscal Repair System approved by the FDA?

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

What company makes TRUESPAN Meniscal Repair System?

TRUESPAN Meniscal Repair System is manufactured by Medos International SARL.

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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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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