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FDA 510(k)

MectaLock TI Triple Loaded Suture Anchor

K-Number: K223582 · 2023-02-24

Decision Date2023-02-24
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MectaLock TI Triple Loaded Suture Anchor is a medical device manufactured by Medacta International S.A.. It received FDA 510(k) clearance on 2023-02-24 under approval number K223582. 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 MectaLock TI Triple Loaded Suture Anchor?

MectaLock TI Triple Loaded Suture Anchor is a medical device that received FDA 510(k) clearance on 2023-02-24. It is manufactured by Medacta International S.A.. The 510(k) number is K223582.

When was MectaLock TI Triple Loaded Suture Anchor approved by the FDA?

MectaLock TI Triple Loaded Suture Anchor received FDA 510(k) clearance on 2023-02-24, under approval number K223582.

What company makes MectaLock TI Triple Loaded Suture Anchor?

MectaLock TI Triple Loaded Suture Anchor is manufactured by Medacta International S.A..

What is the FDA product code for MectaLock TI Triple Loaded Suture Anchor?

The FDA product code for MectaLock TI Triple Loaded Suture Anchor is MBI.

Related PubMed Literature

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.