Y-Knot OneStep Anchor
K-Number: K193606 · 2020-01-22
Device Summary
Frequently Asked Questions
What is the Y-Knot OneStep Anchor?
Y-Knot OneStep Anchor is a medical device that received FDA 510(k) clearance on 2020-01-22. The listed applicant is Conmed Corporation. The 510(k) number is K193606.
When did Y-Knot OneStep Anchor receive FDA 510(k) clearance?
Y-Knot OneStep Anchor received FDA 510(k) clearance on 2020-01-22, under 510(k) number K193606.
Who is the listed applicant for Y-Knot OneStep Anchor?
The FDA 510(k) record lists Conmed Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Y-Knot OneStep Anchor?
The FDA product code for Y-Knot OneStep Anchor is MBI.
Other records listing Conmed Corporation 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: MBI)
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.