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FDA 510(k)

Responsive Arthroscopy Mustang and Mustang Knotless Suture Anchors

K-Number: K222763 · 2022-10-13

ApplicantResponsive Arthroscopy, LLC
Decision Date2022-10-13
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Responsive Arthroscopy Mustang and Mustang Knotless Suture Anchors is a medical device manufactured by Responsive Arthroscopy, LLC. It received FDA 510(k) clearance on 2022-10-13 under approval number K222763. 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 Responsive Arthroscopy Mustang and Mustang Knotless Suture Anchors?

Responsive Arthroscopy Mustang and Mustang Knotless Suture Anchors is a medical device that received FDA 510(k) clearance on 2022-10-13. It is manufactured by Responsive Arthroscopy, LLC. The 510(k) number is K222763.

When was Responsive Arthroscopy Mustang and Mustang Knotless Suture Anchors approved by the FDA?

Responsive Arthroscopy Mustang and Mustang Knotless Suture Anchors received FDA 510(k) clearance on 2022-10-13, under approval number K222763.

What company makes Responsive Arthroscopy Mustang and Mustang Knotless Suture Anchors?

Responsive Arthroscopy Mustang and Mustang Knotless Suture Anchors is manufactured by Responsive Arthroscopy, LLC.

What is the FDA product code for Responsive Arthroscopy Mustang and Mustang Knotless Suture Anchors?

The FDA product code for Responsive Arthroscopy Mustang and Mustang Knotless Suture Anchors is MBI.

Related Clinical Trials

NCT04552119 Safety of Treatment of Shoulder Repair COMPLETED NCT06272201 Incisionless Suture Plications in a POSE2.0 Obesity Study NOT_YET_RECRUITING NCT07491276 Efficacy of Using Knotless Barbed Suture vs N-Butyl Cyanoacrylate Glue Tissue Adhesive for Closure of Intraoral Surgical Incisions ACTIVE_NOT_RECRUITING

Related PubMed Literature

PMID: 40868376 Correlation Analysis of Suture Anchor Pull-Out Strength with Cortical Bone Thickness and Cancellous Bone Density on a Finite Element Model. Bioengineering (Basel, Switzerland) (2025)

Other Devices by Responsive Arthroscopy, LLC

K180573Responsive Arthroscopy Interference Screw System K190446Responsive Arthroscopy Wedge Push-In Suture Anchors K181076Responsive Arthroscopy Wedge Push-In Suture Anchors K180951Responsive Arthroscopy Suture Anchor System K202569Responsive Arthroscopy Interference Screw System K202153Responsive Arthroscopy Suture Anchor System

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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.

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