OSSIOfiber Suture Anchor
K-Number: K213415 · 2022-03-28
Device Summary
Frequently Asked Questions
What is the OSSIOfiber Suture Anchor?
OSSIOfiber Suture Anchor is a medical device that received FDA 510(k) clearance on 2022-03-28. The listed applicant is OSSIO , Ltd.. The 510(k) number is K213415.
When did OSSIOfiber Suture Anchor receive FDA 510(k) clearance?
OSSIOfiber Suture Anchor received FDA 510(k) clearance on 2022-03-28, under 510(k) number K213415.
Who is the listed applicant for OSSIOfiber Suture Anchor?
The FDA 510(k) record lists OSSIO , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OSSIOfiber Suture Anchor?
The FDA product code for OSSIOfiber Suture Anchor is MAI.
Other records listing OSSIO , Ltd. as applicant
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.
Related Devices (Code: MAI)
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.
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.