Y-Knot OneStep Anchor
K-Number: K193606 · 2020-01-22
ApplicantConmed Corporation
Decision Date2020-01-22
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Y-Knot OneStep Anchor is a medical device manufactured by Conmed Corporation. It received FDA 510(k) clearance on 2020-01-22 under approval number K193606. 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 Y-Knot OneStep Anchor?
Y-Knot OneStep Anchor is a medical device that received FDA 510(k) clearance on 2020-01-22. It is manufactured by Conmed Corporation. The 510(k) number is K193606.
When was Y-Knot OneStep Anchor approved by the FDA?
Y-Knot OneStep Anchor received FDA 510(k) clearance on 2020-01-22, under approval number K193606.
What company makes Y-Knot OneStep Anchor?
Y-Knot OneStep Anchor is manufactured by Conmed Corporation.
What is the FDA product code for Y-Knot OneStep Anchor?
The FDA product code for Y-Knot OneStep Anchor is MBI.
Other Devices by Conmed Corporation
Related Devices (Code: MBI)
K163034SUTUREFIX Curved Suture AnchorSmith and Nephew, Inc.
K162198GFS UltimateParcus Medical, LLC
K162386KATOR Suture AnchorKator, LLC
K161033AFX Femoral Implant With InserterCayenne Medical, Inc.
K160996Dunamis Suture Anchor PEEK 3.0mm, 3.5mm, 4.5mm, 5.5mm, 6.5mmDunamis, LLC
K161001MILAGRO ADVANCE PEEK Interference ScrewMedos International SARL
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.