← Product Code [KCY](/submissions/SU/subpart-f%E2%80%94therapeutic-devices/KCY) · K071140 # MRI COMPATIBLE THIGH TOURNIQUET, MODEL C070002 (K071140) _Top Spins, Inc. · KCY · Jun 7, 2007 · General, Plastic Surgery · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/RA/subpart-f%E2%80%94therapeutic-devices/KCY/K071140 ## Device Facts - **Applicant:** Top Spins, Inc. - **Product Code:** [KCY](/submissions/SU/subpart-f%E2%80%94therapeutic-devices/KCY.md) - **Decision Date:** Jun 7, 2007 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 878.5910 - **Device Class:** Class 1 - **Review Panel:** General, Plastic Surgery ## Indications for Use This device is intended for use in MR imaging of peripheral blood yessels in the lower extremity for patients with suspected peripheral vascular disease for diagnostic purposes and pre-operative information. ## Device Story MRI Compatible Thigh Tourniquet; used during MR imaging of lower extremity peripheral blood vessels. Device provides pneumatic compression to occlude blood flow; facilitates diagnostic imaging and pre-operative planning for patients with suspected peripheral vascular disease. Operated by clinical staff in MRI environment. Device design ensures compatibility with magnetic resonance imaging systems; prevents image artifacts and ensures patient safety within high-field magnetic environments. Output is mechanical compression; assists clinicians in visualizing vascular structures by controlling blood flow during scan. ## Clinical Evidence No clinical data provided. Substantial equivalence based on bench testing and design characteristics. ## Technological Characteristics Pneumatic tourniquet system; MRI compatible materials; designed for use in high-field magnetic environments. Class I device under 21 CFR 878.5910. ## Regulatory Identification A pneumatic tourniquet is an air-powered device consisting of a pressure-regulating unit, connecting tubing, and an inflatable cuff. The cuff is intended to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. ## 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}------------------------------------------------ Image /page/0/Picture/0 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized eagle symbol on the right and the text "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" arranged in a circular fashion around the left side of the eagle. The eagle symbol is composed of three curved lines that resemble the wings and body of an eagle. The text is written in uppercase letters and is evenly spaced around the circle. Food and Drug Administration 9200 Corporate Blvd. Rockville MD 20850 JUN - 7 2007 Ms. Erin Buethe Product Manager of MRI Devices TopSpins®, Inc. 403 Riverview Dr. ANN ARBOR MI 48107 Re: K071140 Trade/Device Name: MRI Compatible Thigh Tourniquet Regulation Number: 21 CFR §878.5910 Regulation Name: Pneumatic tourniquet Regulatory Class: I Product Code: KCY Dated: April 17, 2007 Received: April 24, 2007 Dear Ms. Buethe: 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 (Premarket Approval), it may be subject to such 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. Image /page/0/Picture/10 description: The image is a circular logo or emblem. The text "1906-2006" is at the top of the logo. The letters "FDA" are in the center of the logo. The word "Centennial" is below the letters "FDA". There are three stars below the word "Centennial". {1}------------------------------------------------ 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); good manufacturing practice requirements as set forth in the quality systems (OS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Office of Compliance at one of the following numbers, based on the regulation number at the top of this letter: | 21 CFR 876.xxxx | (Gastroenterology/Renal/Urology) | 240-276-0115 | |-----------------|----------------------------------|--------------| | 21 CFR 884.xxxx | (Obstetrics/Gynecology) | 240-276-0115 | | 21 CFR 892.xxxx | (Radiology) | 240-276-0120 | | Other | | 240-276-0100 | Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). 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 (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html Sincerely yours, Nancy C. Brogdon Nancy C. Brogdon Director, Division of Reproductive, Abdominal, and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ ## PREMARKET NOTIFICATION OF MRI COMPATIBLE THIGH TOURNIQUET STATEMENT OF INDICATIONS FOR USE This device is intended for use in MR imaging of peripheral blood yessels in the lower extremity for patients with suspected peripheral vascular disease for diagnostic purposes and pre-operative information. *Prescription Use* Hubert Lerner and (Division Sign-Off) Division of Reproductive, Abdominal, and Radiological Devices 510(k) Number__ --- **Source:** [https://fda.innolitics.com/submissions/RA/subpart-f%E2%80%94therapeutic-devices/KCY/K071140](https://fda.innolitics.com/submissions/RA/subpart-f%E2%80%94therapeutic-devices/KCY/K071140) **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. If you're preparing [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/), [get in touch](https://innolitics.com/contact). **Cite:** Innolitics at https://innolitics.com