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)

KATOR Suture Anchor

K-Number: K173269 · 2018-05-30

ApplicantKator, LLC
Decision Date2018-05-30
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KATOR Suture Anchor is a medical device manufactured by Kator, LLC. It received FDA 510(k) clearance on 2018-05-30 under approval number K173269. 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 KATOR Suture Anchor?

KATOR Suture Anchor is a medical device that received FDA 510(k) clearance on 2018-05-30. It is manufactured by Kator, LLC. The 510(k) number is K173269.

When was KATOR Suture Anchor approved by the FDA?

KATOR Suture Anchor received FDA 510(k) clearance on 2018-05-30, under approval number K173269.

What company makes KATOR Suture Anchor?

KATOR Suture Anchor is manufactured by Kator, LLC.

What is the FDA product code for KATOR Suture Anchor?

The FDA product code for KATOR Suture Anchor is MBI.

Other Devices by Kator, LLC

K162386KATOR Suture Anchor

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.

↑