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FDA 510(k)

LigaMetrics Suture Anchors

K-Number: K171964 · 2017-09-19

ApplicantMortise Medical, LLC
Decision Date2017-09-19
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LigaMetrics Suture Anchors is a medical device manufactured by Mortise Medical, LLC. It received FDA 510(k) clearance on 2017-09-19 under approval number K171964. 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 LigaMetrics Suture Anchors?

LigaMetrics Suture Anchors is a medical device that received FDA 510(k) clearance on 2017-09-19. It is manufactured by Mortise Medical, LLC. The 510(k) number is K171964.

When was LigaMetrics Suture Anchors approved by the FDA?

LigaMetrics Suture Anchors received FDA 510(k) clearance on 2017-09-19, under approval number K171964.

What company makes LigaMetrics Suture Anchors?

LigaMetrics Suture Anchors is manufactured by Mortise Medical, LLC.

What is the FDA product code for LigaMetrics Suture Anchors?

The FDA product code for LigaMetrics 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

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 Mortise Medical, LLC

K172620SyndesMetrics Syndesmosis Repair System

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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