← Product Code [DQY](/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQY) · K033320 # SCOUT PRO (K033320) _Biotronik, Inc. · DQY · Nov 19, 2003 · Cardiovascular · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQY/K033320 ## Device Facts - **Applicant:** Biotronik, Inc. - **Product Code:** [DQY](/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQY.md) - **Decision Date:** Nov 19, 2003 - **Decision:** SESE - **Submission Type:** Special - **Regulation:** 21 CFR 870.1250 - **Device Class:** Class 2 - **Review Panel:** Cardiovascular - **Attributes:** Therapeutic ## Indications for Use The intended use of the SCOUTPro is for introducing leads into the vessels of the left heart via the coronary sinus. ## Device Story ScoutPro is a percutaneous catheter system designed to facilitate access to and probing of the coronary sinus for lead placement in the left heart. It is an expanded and modified version of the predicate SCOUT system. The device consists of various configurations including guiding catheters (BIO 1, BIO 2, Hook, Multi-Purpose Hook, Amplatz 6.0), dilators, peel-away sheaths, guide wires, needles, syringes, and slitter tools. It is used by clinicians in a clinical setting to assist in the navigation and introduction of cardiac leads. The device functions as a mechanical delivery system; it does not involve electronic processing, software, or automated decision-making. By providing specialized catheter shapes and accessory tools, it enables physicians to navigate the venous system to the coronary sinus, facilitating cardiac pacing or defibrillation lead implantation. ## Clinical Evidence Bench testing only. ## Technological Characteristics Percutaneous catheter system; includes guiding catheters, dilators, peel-away sheaths, guide wires, needles, syringes, and slitter tools. Mechanical device; no energy source, software, or electronic components. Sterilization method not specified. ## Regulatory Identification A percutaneous catheter is a device that is introduced into a vein or artery through the skin using a dilator and a sheath (introducer) or guide wire. ## Predicate Devices - SCOUT ([K020821](/device/K020821.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}------------------------------------------------ Image /page/0/Picture/1 description: The image shows the text "KO33320" in a bold, handwritten-like font. Below this, the date "October 13, 2003" is printed in a clear, sans-serif font. The text and date are aligned to the left, creating a simple yet informative composition. The image appears to be a scan or a digital capture of a document or label. # ScoutPro Special 510(k) Premarket Notification #### 510(k) SUMMARY 1. Name and Address of Sponsor: NOV 1 9 2003 BIOTRONIK, Inc. 6024 Jean Road Lake Oswego, OR 97035 Establishment Registration Number: 1028232 Device Name: Proprietary Name: Classification: Classification Name: Product Code: ScoutPro Class II (21 CFR 870.1250) Percutaneous Catheter DQY ### General Description: The ScoutPro is designed to assist with introducing leads into the vessels of the left heart via the coronary sinus. It facilitates access to the coronary sinus venous system as well as probing of the coronary sinus. The ScoutPro has been expanded and modified from BIOTRONIK's currently legally marketed SCOUT (K020821, 06-03-02). The following ScoutPro accessories are the subjects of this 510(K); ScoutPro 8F that contains the following components: - . 1 hemostatic valve - . 2 guiding catheters BIO 1 and BIO 2 - 1 dilator for the quiding catheter . - 1 peel-away sheath 11F - 1 guide wire ● - 1 needle . - 1 svringe - 2 slitter tools 4.9 F and 6.3 F for different lead sizes ● ScoutPro Sheath "Hook" that contains the following components: - . 1 quiding catheter "Hook" - 1 dilator for the guiding catheter . ScoutPro Sheath "Multi-Purpose Hook" that contains the following components: - 1 guiding catheter "Multi-Purpose Hook" . - 1 dilator for the guiding catheter . ScoutPro Sheath "Amplatz 6.0" contains the following components: - . 1 quiding catheter "Amplatz 6.0" - . 1 dilator for the guiding catheter ## Indication for Use: The intended use of the ScoutPro is for introducing leads into the vessels of the left heart via the coronary sinus. {1}------------------------------------------------ Name and Address of Manufacturers: BIOTRONIK GmbH & Co. KG (reg. no. 9610139) Woermannkehre 1, 12359 Berlin, Germany 011-49-30-689-05-304 > BIOTRONIK AG (reg. no. 8043892) Ackerstrasse 6 8180 Bülach, Switzerland 011-41-1-864-5169 #### Contact Person(s) and Phone Number: Jon Brumbaugh Director, Regulatory Affairs Phone (888) 345-0374 Fax (503) 635-9936 {2}------------------------------------------------ Image /page/2/Picture/2 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the perimeter. Inside the circle is a stylized image of an eagle or bird-like figure, composed of three curved lines that suggest the head, body, and tail feathers. NOV 1 9 2003 Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 BIOTRONIK, Inc. c/o Mr. Jon Brumbaugh Director, Regulatory Affairs 6024 Jean Road Lake Oswego, OR 97035 Re: K033320 Trade Name: SCOUTPro Regulation Number: 21 CFR 870.1250 Regulation Name: Percutaneous Catheter Regulatory Class: Class II (two) Product Code: DOY Dated: October 13, 2003 Received: October 15, 2003 Dear Mr. Brumbaugh: 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 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. {3}------------------------------------------------ Page 2 - Mr. Jon Brumbaugh 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 (QS) 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 (301) 594-4646. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 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/dsma/dsmamain.html Sincerely yours, Mede May Bram D. Zuckerman, M.D. Director Division of Cardiovascular Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {4}------------------------------------------------ l ﺴﺮ Page of 510(k) Number (if known): Device Name:_SCOUTPro Indications For Use: The intended use of the SCOUTPro is for introducing leads into the vessels of the left heart via the coronary sinus. (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) CMessis Mun for BDE (Division Sign-Off) Division of Cardiovascular Devices 510(k) number K033202 (Optional Format 3-10-98) ------------------------------------------------------------------------------------------------------------------------------------------------------------------------------ - --- **Source:** [https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQY/K033320](https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DQY/K033320) **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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