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FDA 510(k)

MD Mattress Suture Placement Device

K-Number: K222783 · 2024-01-12

ApplicantLsi Solutions, Inc.
Decision Date2024-01-12
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MD Mattress Suture Placement Device is the device name listed in this FDA 510(k) record. The listed applicant is Lsi Solutions, Inc.. It received FDA 510(k) clearance on 2024-01-12 under 510(k) number K222783. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MD Mattress Suture Placement Device?

MD Mattress Suture Placement Device is a medical device that received FDA 510(k) clearance on 2024-01-12. The listed applicant is Lsi Solutions, Inc.. The 510(k) number is K222783.

When did MD Mattress Suture Placement Device receive FDA 510(k) clearance?

MD Mattress Suture Placement Device received FDA 510(k) clearance on 2024-01-12, under 510(k) number K222783.

Who is the listed applicant for MD Mattress Suture Placement Device?

The FDA 510(k) record lists Lsi Solutions, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MD Mattress Suture Placement Device?

The FDA product code for MD Mattress Suture Placement Device is GCJ.

Other records listing Lsi Solutions, Inc. 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.

K202551Cor-Knot MicroK203120RD QUICK LOAD SUTURE, 0 Polyester, RD QUICK LOAD SUTURE, 2-0 Polyester, RD QUCIK LOAD SUTURE, 2-0 PolypropyleneK203081RAM COR-SUTURE QUCIK LOAD Surgical Suture, COR-SUTURE QUICK LOAD Surgical SutureK163639LS-5 ePTFE Suture

Related Devices (Code: GCJ)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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