Arthrex SwiveLock Suture Anchor
K-Number: K193503 · 2020-01-15
Device Summary
Frequently Asked Questions
What is the Arthrex SwiveLock Suture Anchor?
Arthrex SwiveLock Suture Anchor is a medical device that received FDA 510(k) clearance on 2020-01-15. It is manufactured by Arthrex, Inc.. The 510(k) number is K193503.
When was Arthrex SwiveLock Suture Anchor approved by the FDA?
Arthrex SwiveLock Suture Anchor received FDA 510(k) clearance on 2020-01-15, under approval number K193503.
What company makes Arthrex SwiveLock Suture Anchor?
Arthrex SwiveLock Suture Anchor is manufactured by Arthrex, Inc..
What is the FDA product code for Arthrex SwiveLock Suture Anchor?
The FDA product code for Arthrex SwiveLock Suture Anchor is MAI.
Related Clinical Trials
Other Devices by Arthrex, Inc.
Related Devices (Code: MAI)
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.