← Product Code [ITI](/submissions/PM/subpart-d%E2%80%94physical-medicine-prosthetic-devices/ITI) · K041211 # POWERED WHEELCHAIR, MODEL C-1000 (K041211) _Otto Bock Healthcare LP · ITI · Oct 1, 2004 · Physical Medicine · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/PM/subpart-d%E2%80%94physical-medicine-prosthetic-devices/ITI/K041211 ## Device Facts - **Applicant:** Otto Bock Healthcare LP - **Product Code:** [ITI](/submissions/PM/subpart-d%E2%80%94physical-medicine-prosthetic-devices/ITI.md) - **Decision Date:** Oct 1, 2004 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 890.3860 - **Device Class:** Class 2 - **Review Panel:** Physical Medicine - **Attributes:** Therapeutic ## Indications for Use The C-1000 is front wheel drive powered wheelchair for active users. These wheelchairs provide mobility to physically challenged persons. The wheelchair can be moved by the user operating the remote control. The wheelchair can also be pushed by an assistant grasping the handles attached to the back rest. ## Device Story C-1000 is a front-wheel-drive powered wheelchair for active users; features 'H' frame design. Input: user commands via remote control. Transformation: electronic controller (Curtis Instruments MC-2) manages micro motor and regenerative disc brakes to drive wheels. Output: powered mobility for user; manual push capability via backrest handles for assistants. Used in various environments by physically challenged individuals. Benefits: provides independent mobility for users with limited sitting capacity. ## Clinical Evidence Bench testing only. Device tested by TÜV Product Service for compliance with EN 12184, ISO 7176 series, and ANSI/RESNA WA Vol. 2 Section 21 (1998) for EMC. Results confirmed the test sample fulfilled all requirements. ## Technological Characteristics Front-wheel-drive powered wheelchair; 'H' frame construction. Components include Curtis Instruments MC-2 electronic controller, micro motor, and regenerative disc brakes. Tested to EN 12184, ISO 7176 series, and ANSI/RESNA standards for safety and EMC. ## Regulatory Identification A powered wheelchair is a battery-operated device with wheels that is intended for medical purposes to provide mobility to persons restricted to a sitting position. ## Predicate Devices - Chairman ([K960951](/device/K960951.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}------------------------------------------------ Otto Bock HEALTH CARE K041211 OCT 1 - 2004 #### 510(k) Summary # 510(k) SUMMARY of SAFETY and EFFECTIVENESS #### A. General Information | 1. Submitter's Name: | OTTO BOCK HealthCare LP | |-------------------------|-----------------------------------------------------------------| | 2. Address: | Two Carlson Parkway N., Suite 100
Minneapolis, MN 55447-4467 | | 3. Telephone: | 763-489-5105 | | 4. Contact Person: | Bob Clarke | | 5. Date Prepared: | April 12, 2004 | | 6. Registration Number: | 2182293 | | Device | | ## B. 1. Name: C-1000 Powered Wheelchair 2. Trade Name: C-1000 Powered Wheelchair 3. Common Name: Powered wheelchair 4. Classification Name: Powered wheelchair 5. Product Code: ITI 6. Class: I I 7. Regulation Number: 890.3860 #### QUALITY FOR LIFE North American Headquarters Two Carlson Parkway N., Suite Minneapolis, MN 55447-4467 Phone 1.800.328.4058 Fax 1.800.655.4963 Customer Support & Distribution Center 14630 28t Avenue North Minneapolis, MN 55447-4821 Phone 1.800.328.4058 Fax 1.800.962.2549 Technical Center 14800 28th Avenue North, Suite Minneapolis, MN 55447-4873 Phone 1.800.795.8846 Fax 1.800.810.7994 Florida Area Fabrication Center 755 Clay Street Winter Park, FL 32789 Phone 1.800.354.5418 Fax 1.407.599.7999 Ohio Area Fabrication Center 84 Westpark Road Centerville, OH 45459 Phone 1.937.432.0082 Fax 1.937.432.0087 Utah Design & Manufacturing Center 3820 W. Great Lakes Drive Salt Lake City, UT 84120-7205 Phone 1.801.956.2400 Fax 1.801.956.2401 Minnesota Design & Manufacturing Center 820 Sundial Drive Waite Park, MN 56387 Phone 1.800.688.4832 Fax 1.320.251.0110 Customer Satisfaction Hotline 1.877.OBSOLVE 1.877.627.6583 www.ottobockus.com {1}------------------------------------------------ Image /page/1/Picture/0 description: The image shows the logo for Otto Bock Health Care. The words "Otto Bock" are written in a cursive font, with a line underneath. Below the line, the words "HEALTH CARE" are written in a sans-serif font. ### C. Identification of Legally Marketed Devices | 1. Name: | Chairman | |------------------|----------------| | 2. K Number: | K960951 | | 3. Date Cleared: | April 30, 1997 | ### D. Description of the Device The C-1000 Powered Wheelchair is a front wheel drive powered wheelchair, manufactured in Germany at production facilities of OTTO BOCK HealthCare. The C-1000 has an "H" frame, controlled by a Curtis Instruments MC-2, clectronic regenerative disc brakes and Micro Motor. #### E. Intended Use Statement The C-1000 is front wheel drive powered wheelchair for active users. These wheelchairs provide mobility to physically challenged persons. The wheelchair can be moved by the user operating the remote control. The wheelchair can also be pushed by an assistant grasping the handles attached to the back rest. #### F. Technological Characteristics Summary The C-1000 Wheelchair is substantially equivalent to the Permobil AB Chairman Wheelchair, cleared on April 30, 1997 as K960951. Each wheelchair is a powered wheelchair for the active user, with a rigid frame and similar characteristics. The C-1000 was tested by TÜV Product Service to the following standards: - EN 12184 - ISO 7176 Series . - ANSI/RESNA WA Vol. 2 Section 21 Amendments 1998 for EMC . with the conclusion that "the test sample fulfills the requirements." #### QUALITY FOR LIFE North American Headquarters Two Carlson Parkway N., Suite Minneapolis, MN 55447-4467 Phone 1.800.328.4058 Fax 1.800.655.4963 Customer Support & Distribution Center 14630 28th Avenue North Minneapolis, MN 55447-482 Phone 1.800.328.4058 Fax 1.800.962.2549 Technical Center 14800 28th Avenue North, Suite Minneapolis, MN 55447-487 Phone 1,800,795,8846 Fax 1.800.810.7994 Florida Area Fabrication Cente 55 Clay Street Vinter Park, FL 32789 Phone 1.800.354.5418 Fax 1-407.599.7999 Ohio Area Fabrication Cente Westpark Road enterville, OH 45459 Phone 1.937.432.0082 x 1.937.432.0087 Itah Design & anufacturing Center 820 W. Great Lakes Drive alt Lake City, UT 84120-72 Phone 1.801.956.2400 ax 1.801.956.2401 innesota Design & anufacturing Center 20 Sundial Drive Vaite Park, MN 56387 hone 1.800.688.4832 ax 1.320.251.0110 Customer Satisfaction Hotline 1.877.OBSOLVE 1.877.627.6583 www.ottobockus.com {2}------------------------------------------------ Image /page/2/Picture/1 description: The image is a black and white seal for the Department of Health & Human Services - USA. The seal is circular with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. In the center of the seal is a stylized caduceus symbol, which is a symbol of medicine and health. The caduceus is made up of three intertwined snakes and a staff. Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 OCT 1 - 2004 Otto Bock HealthCare, LP C/o Mr. William Jackson W.F. Jackson Associates, Limited 2247 Jennifer Lane St. Paul, Minnesota 55109-2851 Re: K041211 Trade/Device Name: C-1000 Powered Wheelchair Regulation Number: 21 CFR 890.3860 Regulation Name: Powered Wheelchair Regulatory Class: Class II Product Code: ITI Dated: September 18, 2004 Received: September 22, 2004 Dear Mr. Jackson: 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 for associated in 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. 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. {3}------------------------------------------------ Page 2 - Mr. William Jackson This letter will allow you to begin marketing your device as described in your Section 510(k) I his icher will anow you to began mailing of substantial equivalence of your device to a legally premaince notification. " 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 if you dosire of Compliance at (240) 276-0120. Also, please note the regulation entitled, eonading 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 other general 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, Mark A. Mellem Celia M. Witten, PhD, MD Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {4}------------------------------------------------ ## Indications for Use 510(k) Number (if known): K041211 Device Name: C-1000 Powered Wheelchair Indications for Use: - Provide mobility to persons physically challenged and limited to sitting . position. Prescription Use (Part 21 CFR 801 Subpart D) AND/OR Over-The-Counter Use X (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) Mark N Melbern al. Restorative, Division of Gener Divisions of Occal Devices 510(k) Number- Page 1 of 1 1041211 --- **Source:** [https://fda.innolitics.com/submissions/PM/subpart-d%E2%80%94physical-medicine-prosthetic-devices/ITI/K041211](https://fda.innolitics.com/submissions/PM/subpart-d%E2%80%94physical-medicine-prosthetic-devices/ITI/K041211) **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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