Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Arthrex SwiveLock Suture Anchor

K-Number: K193503 · 2020-01-15

ApplicantArthrex, Inc.
Decision Date2020-01-15
Product CodeMAI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Arthrex SwiveLock Suture Anchor is a medical device manufactured by Arthrex, Inc.. It received FDA 510(k) clearance on 2020-01-15 under approval number K193503. The device is classified under product code MAI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 168 devices →

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.