← Product Code LXC · K090961 # TWIN STAR COMPARTMENT PRESSURE MONITOR AND FLUID COLLECTION CATHETER SYSTEM (CMS-II) (K090961) _Twin Star Medical, Inc. · LXC · Jun 12, 2009 · OR · SESE_ **Canonical URL:** https://fda.innolitics.com/device/K090961 ## Device Facts - **Applicant:** Twin Star Medical, Inc. - **Product Code:** LXC - **Decision Date:** Jun 12, 2009 - **Decision:** SESE - **Submission Type:** Traditional - **Device Class:** Class U - **Review Panel:** OR ## Intended Use The Twin Star Compartment Pressure Monitor and Fluid Collection Catheter System (CMS-II) is intended for the immediate or continuous measurement of intracompartmental pressures and/or the withdrawal of fluid for subsequent analysis. The measured compartmental pressures can be used as an aid in the diagnosis of compartment syndrome. ## Device Story System consists of introducer (tear-away sheath over stainless steel trocar), pressure monitoring and fluid collection (PMFC) catheter, fluid collection (FC) catheter, and compartment pressure monitor. Introducer facilitates placement of indwelling catheter into muscle compartment. Catheter monitors intramuscular pressure and allows interstitial fluid sampling for up to 24 hours. Monitor displays intracompartmental pressure. Used in clinical settings to aid compartment syndrome diagnosis. Provides healthcare providers with real-time pressure data to inform clinical decision-making and patient management. ## Clinical Evidence Bench testing only. Evidence includes biocompatibility, electrical safety testing, and design verification. Risk analysis and software validation were conducted to confirm system operations. ## Technological Characteristics System includes stainless steel trocar, plastic tear-away sheath, and indwelling catheters. Features include pressure sensing, fluid collection capability, and electronic pressure display. Single-patient use. Electrical safety testing performed. Software-based system operations validated. ## Predicate Devices - Twin Star Compartment Monitoring and Fluid Collection Catheter System (Catheter, [K041771](/device/K041771.md)) - Twin Star Compartment Pressure Monitoring and Fluid Collection Monitor (CMS Monitor, [K060963](/device/K060963.md)) - Synthes (USA) Compartmental Pressure Monitoring System ([K031555](/device/K031555.md)) - Stryker Compartment Syndrome Pressure Monitoring System ([K844214](/device/K844214.md)) ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0}------------------------------------------------ K090961 Page / of 2 i Carlos Career : 上 :: : 上一篇: ## JUN 1 2 2009 ## 510(k) Summary | Twin Star Compartment Pressure Monitor and Fluid Collection Catheter System
(CMS-II) | | | |-----------------------------------------------------------------------------------------|----------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | | 510(k) Summary | This summary of 510(k) safety and effectiveness information is
being submitted in accordance with the requirements of 21
C.F.R § 807.92. | | | Applicant | Twin Star Medical, Inc. | | | Submitter | Twin Star Medical, Inc.
1000 Westgate Drive, Suite 117
St. Paul, MN 55114
Tel: 612-990-0631
Fax: 651-209-0556 | | | Contact Person | Jim Stice, President / CEO | | | Date Prepared | March 27, 2009 | | | Device Trade Name | Twin Star Compartment Pressure Monitor and Fluid Collection
Catheter System (CMS-II) | | | Device Common Name | Monitor, Pressure, Intracompartmental | | | Classification Name | Unclassified, Product Code LXC | | | Classification Panel | Orthopedic | | | Predicate Devices | Twin Star Compartment Monitoring and Fluid Collection
Catheter System (Catheter, K041771), Twin Star Compartment
Pressure Monitoring and Fluid Collection Monitor (CMS
Monitor, K060963), Synthes (USA) Compartmental Pressure
Monitoring System (K031555), Stryker Compartment Syndrome
Pressure Monitoring System (K844214). | | | Intended use | The Twin Star Compartment Pressure Monitor and Fluid
Collection Catheter System (CMS-II) is intended for the
immediate or continuous measurement of intracompartmental
pressures and/or the withdrawal of fluid for subsequent
analysis. The measured compartmental pressures can be used
as an aid in the diagnosis of compartment syndrome. | | | Device Description | The Twin Star Compartment Pressure Monitoring and Fluid
Collection Catheter System (CMS-II) consists of four major
components; an Introducer, a Pressure Monitoring and Fluid
Collection (PMFC) Catheter, a Fluid Collection (FC) Catheter,
and a Compartment Pressure Monitor. The Introducer consists
of tear-away plastic sheath placed over a stainless steel trocar. | 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - : : : {1}------------------------------------------------ K090961 Page 2 of 2 compartment to facilitate the placement of the indwelling Pressure Monitoring Fluid Collection / Fluid Collection catheter. The indwelling Catheter is designed to monitor intramuscular compartment pressure as well as provide a means to sample interstitial fluid for laboratory analysis. The indwelling Catheter is designed for use up to 24 hours. The Twin Star Compartment Pressure Monitoring provides a means of displaying the intracompartmental pressure. Bench testing was performed to support a determination of substantial equivalence and consisted of biocompatibility, electrical safety testing and design verification. Results from this testing provide assurance that the proposed device has been designed and tested to assure conformance to the requirements for its intended use. A risk analysis of the system and its software was performed and testing was conducted to validate the systems overall operations. The Twin Star Compartment Pressure Monitor and Fluid Collection Catheter System (CMS-II) utilizes substantially equivalent performance attributes and safety components as the predicate devices. It shares the following similarities to the predicate devices: - Monitoring Pressure . - Fluid Collection - Membrane Diameter - Single Patient Use . - Pressure Sensor Location - Electrical Safety . - Vacuum Source - Principles of operation Based on the similar indications for use, technological characteristics and performance testing, Twin Star Medical, Inc. believes the proposed device, the Twin Star Compartment Pressure Monitor and Fluid Collection Catheter System (CMS-II), is substantially equivalent to the Twin Star Compartment Monitoring and Fluid Collection Catheter System (Catheter, K041771). Twin Star Compartment Pressure Monitoring and Fluid Collection Monitor (CMS Monitor, K060963), Synthes (USA) Compartmental Pressure Monitoring System (K031555) and the Stryker Compartment Syndrome Pressure Monitoring System (K844214). Performance data Summary of Substantial Equivalence Conclusion {2}------------------------------------------------ Image /page/2/Picture/0 description: The image shows the logo for the Department of Health & Human Services - USA. The logo is a circular seal with the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the perimeter. Inside the circle is an abstract symbol that resembles an eagle or bird in flight. The symbol is composed of three curved lines that form the wings and body of the bird. ## DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 Twin Star Medical, Incorporated % Sachs & Associates, Incorporated Mr. Gregory W. Sachs President 5116 Birch Road Minnetonka, Minnesota 55345 JUN 1 2 2009 Re: K090961 · Trade/Device Name: Twin Star Compartment Pressure Monitor and Fluid Collection Catheter System (CMS-II) Regulatory Class: II Product Code: LXC Dated: May 14, 2009 Received: May 15, 2009 Dear Mr. Sachs: We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); {3}------------------------------------------------ Page 2-Mr. Gregory W. Sachs and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act): 21 CFR 1000-1050. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHQffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to http://www.fda.gov/cdrh/mdr/ for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance. You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (240) 276-3150 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html. Sincerely vours. Mark N. Melkerson Division of Surgical. Orthoped and Restorative Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {4}------------------------------------------------ Image /page/4/Picture/0 description: The image shows the text "k 090961" on the first line and "Page 1 of 1" on the second line. The text appears to be handwritten. The numbers "090961" and "1 of 1" are clearly visible. The letter "k" is also clearly visible. Page 1 of 1 ## Indications for Use Statement 510(k) Number (if known): ____________________________________________________________________________________________________________________________________________________ Device Name: Twin Star Compartment Pressure Monitor and Fluid Collection Catheter System (CMS-II) Indications for Use: The Twin Star Compartment Pressure Monitor and Fluid Collection Catheter System (CMS-II) is intended for the immediate or continuous measurement of intracompartmental pressures and/or the withdrawal of fluid for subsequent analysis. The measured compartmental pressures can be used as an aid in the diagnosis of compartment syndrome. Prescription Use X (Part 21 CFR 801 Subpart D) AND/OR Over-The-Counter Use (21 CFR 801 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) (Division Sign-Off) Division of Surgical, Orthopedic, and Restorative Devices 510(k) Number K090961 --- **Source:** [https://fda.innolitics.com/device/K090961](https://fda.innolitics.com/device/K090961) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. 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