Modular Power Standing System

K191376 · Motion Concepts · IPL · Aug 13, 2019 · Physical Medicine

Device Facts

Record IDK191376
Device NameModular Power Standing System
ApplicantMotion Concepts
Product CodeIPL · Physical Medicine
Decision DateAug 13, 2019
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 890.3900
Device ClassClass 2

Intended Use

The Modular Power Standing System is appropriate for use by individuals who drive a power wheelchair and cannot stand up on their own. The Modular Power Standing System allows such users to change position including from seating to standing, standing to seating, or any position in between. The device is appropriate for indoor and outdoor use. Motion Concepts makes no claims as to the therapeutic effectiveness of the products. Our only claims relate to the ability of the products to provide safe and reliable powered repositioning on the equipment onto which they are installed.

Device Story

Modular Power Standing System (MPSS) is a seating system for attachment to power wheelchair bases; provides power stand-up, tilt (0°-45°), recline (90°-178°), and seat elevation (6.5 inches). Operated via switches or powerbase joystick. Uses electro-mechanical linear actuators to drive linkages; includes knee and chest supports for standing stability. Used in private residences, chronic care facilities, indoors, and outdoors. Safety features include drive lock-out, reduced drive mode when positioned beyond limits, and front castor locks for standing stability. Electrical components are 24VDC with current limiting. Benefits include improved reach, accessibility, and repositioning for users unable to stand independently.

Clinical Evidence

No clinical data. Bench testing only. Includes biocompatibility (ISO 10993-5, ISO 10993-10), mechanical performance (ISO 7176 series), electrical safety, and EMC (ISO 7176-21).

Technological Characteristics

Materials: laser-cut steel, steel tube, machined aluminum, powder-coated. Actuation: 24VDC electro-mechanical linear actuators. Connectivity: interfaces with powerbase joystick or switches. Standards: ISO 7176 series (stability, brakes, energy, dimensions, speed, fatigue, climatic, obstacle, control systems, EMC). Biocompatibility: ISO 10993-5/10. Software: Moderate level of concern.

Indications for Use

Indicated for individuals who drive a power wheelchair and cannot stand up on their own, including those with spinal cord injury, spina bifida, cerebral palsy, multiple sclerosis, muscular dystrophy, polio, rheumatism, or other conditions requiring power wheelchair use and inability to shift weight.

Regulatory Classification

Identification

A standup wheelchair is a device with wheels that is intended for medical purposes to provide mobility to persons restricted to a sitting position. The device incorporates an external manually controlled mechanical system that is intended to raise a paraplegic to an upright position by means of an elevating seat.

Predicate Devices

Reference Devices

Related Devices

Submission Summary (Full Text)

{0}------------------------------------------------ Image /page/0/Picture/0 description: The image contains the logo of the U.S. Food and Drug Administration (FDA). The logo consists of two parts: the Department of Health & Human Services seal on the left and the FDA acronym with the full name of the agency on the right. The FDA part is in blue, with the acronym in a square and the full name, "U.S. Food & Drug Administration," written out in a clear, sans-serif font. August 13, 2019 Motion Concepts Dona Bhamra Senior Quality and Regulatory Affairs Manager 84 Citation Drive, Unit #1 Concord, L4K 3C1 Canada Re: K191376 Trade/Device Name: Modular Power Standing System Regulation Number: 21 CFR 890.3900 Regulation Name: Standup Wheelchair Regulatory Class: Class II Product Code: IPL Dated: May 17, 2019 Received: May 23, 2019 Dear Dona Bhamra: 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. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database located at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. 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. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading. 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 {1}------------------------------------------------ requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting of medical device-related adverse events) (21 CFR 803) for devices or postmarketing safety reporting (21 CFR 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (OS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems. For comprehensive regulatory information about mediation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100). Sincerely, for Vivek J. Pinto. PhD Assistant Director DHT5B: Division of Neuromodulation and Physical Medicine Devices OHT5: Office of Neurological and Physical Medicine Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ ## Indications for Use 510(k) Number (if known) K191376 ### Device Name Modular Power Standing System (MPSS) ## Indications for Use (Describe) The Modular Power Standing System is appropriate for use by individuals who drive a power wheelchair and cannot stand up on their own. The Modular Power Standing System allows such users to change position including from seating to standing, standing to seating, or any position in between. The device is appropriate for indoor and outdoor use. Motion Concepts makes no claims as to the therapeutic effectiveness of the products. Our only claims relate to the ability of the products to provide safe and reliable powered repositioning on the equipment onto which they are installed. | Type of Use (Select one or both, as applicable) | | |-------------------------------------------------|--| |-------------------------------------------------|--| | | Prescription Use (Part 21 CFR 801 Subpart D) |X Over-The-Counter Use (21 CFR 801 Subpart C) ## CONTINUE ON A SEPARATE PAGE IF NEEDED. This section applies only to requirements of the Paperwork Reduction Act of 1995. ## *DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.* The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to: > Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff@fda.hhs.gov "An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number." {3}------------------------------------------------ This summary of 510(k) safety and effectiveness information is submitted in accordance with the requirements of 21 CFR 807.92 #### l. SUBMITTER II. III. | FDA Establishment Registration Number: | 9615350 | |----------------------------------------|---------------------------------------------------------------------------| | Address: | Motion Concepts<br>84 Citation Drive, Unit 1<br>Concord, Ontario, L4K 3C1 | | Phone: | 905-695-0134 | | Fax: | 905-695-0138 | | Contact person: | Dona Bhamra | | Date Summary Prepared: | 1-Aug-2019 | | <b>DEVICE</b> | | |----------------------------|--------------------------------------| | Device Proprietary Name: | Modular Power Standing System (MPSS) | | Common Name: | Standup Wheelchair | | Classification Regulation: | 21 CFR, 890.3900 | | Product Code: | IPL | | Classification of Device: | Class II | | <b>PREDICATE DEVICE</b> | | |-------------------------|--------------------------------------------------| | Predicate Device: | Levo C3 Power Wheelchair | | | K083017 | | | Product Code IPL | | | 21 CFR 890.3900 | | Reference Device: | Motion Concepts Modular Power Positioning System | | | K150574 | | | Product Code ITI | | | 21 CFR 890.3860 | #### IV. DEVICE DESCRIPTION The Modular Power Standing System (MPSS) is a seating system which is added to a wheelchair powerbase to provide four basic functions: power stand-up, power tilt, power recline including shear reduction, and power elevate. It can be operated in private residences, chronic care facilities, indoor and outdoors. Note the MPSS in itself does not include any wheelchair base components such as wheelchair frame, drive controls, wheels, brakes, batteries, suspension etc. The Stand function is used to orient the user in an upright position. The mechanism consists of linkages driven by linear actuators. The system includes both a knee support to help stabilize the user in the standing position. The Tilt function is used to change the seating inclination angle of user. The mechanisms consist of linkages driven by linear actuators. The range of tilt is 0° to 45°. {4}------------------------------------------------ 510(k) Summary Modular Power Standing System The Recline function causes the position of the occupant's back to change by changing the position of the backrest with respect to the seat pan. The Shear Reduction works in conjunction with Recline to reduce the shear movement between the user and the backrest. The mechanisms consist of linkages driven by linear actuators. The range of Recline is 90° to 178°. The Elevating seat module allows the user to elevate the entire seat. The mechanisms consist of linkages driven by linear actuators. The range of elevation is 6.5 inches. The maximum occupant weight for the system is 250 lb. The Modular Power Standing System is assembled using primarily laser-cut steel parts, steel tube, machined aluminum, and mounting hardware. The various power positioning modules may be activated via two options: using switches or through the powerbase manufacturer supplied joystick. Safety features include a drive lock-out and reduced drive mode which are activated when any of the power functions are activated beyond pre-set limits. The system also includes front castor locks to provide additional front stability when in stand mode. Electrical components are maximum 24 volts and include current limiting within the seat control box. Stability of the Modular Power Standing System was tested on the powerbase selected for this application. These tests were conducted to ensure the safety of the power wheelchair was not compromised by the addition of the Modular Power Standing System. #### V. INDICATIONS FOR USE The Modular Power Standing System is appropriate for use by individuals who drive a power wheelchair and cannot stand up on their own. The Modular Power Standing System allows such users to change position including from seating to standing to seating, or any position in between. The device is appropriate for indoor and outdoor use. Motion Concepts makes no claims as to the therapeutic effectiveness of the products. Our only claims relate to the ability of the provide safe and reliable powered repositioning on the equipment onto which they are installed. #### VI. COMPARISON OF TECHNOLOGICAL CHARACTERISTICS WITH THE PREDICATE DEVICE The new Modular Power Standing System was designed to add the standing function option to the existing Motion Concepts Modular Power Positioning System functions of tilt, recline, and elevate. This new standing feature functions similarly to the Levo C3 K083017, which will therefore serve as the Predicate device. In order to further demonstrate safety and effectiveness the Modular Power Position System K150574 will also be used as a reference device. ## Predicate device: Levo C3 (K083017) Both the subject device Modular Power Standing System (MPSS) and the predicate device Levo C3 Power Wheelchair are systems which provide a stand-up feature, allowing users to reposition themselves from seating to standing and vice versa. Both systems include both a knee support to help stabilize the user in the standing position. The two systems are equivalent with respect to the following: - ー indications for use - ー target population {5}------------------------------------------------ 510(k) Summary Modular Power Standing System - safety features l - general design - use of materials l - standards met The seat size (width/depth/back height) differs in that the MPSS does not offer the smaller seat sizes offered on the predicate device. This difference does not affect the effectiveness of the MPSS over the range offered. ## Reference Device Motion Concepts Modular Power Position System (K150574) Both the subject device Modular Power Standing System (MPSS) and reference device Modular Positioning System are seating systems that provide three basic functions: power recline including shear reduction and power elevate. The two systems are equivalent with respect to the following: - safety features l - electrical safety - general design - use of materials - | energy used - motor type used - standards met । The seat size (width/depth/back height) differs in that the MPSS does not offer the larger seat sizes offered on the referenced device. This difference does not affect the effectiveness of the MPSS over the range offered. The elevate range on the referenced device is less than that offered on the MPSS, however the effectiveness is maintained as the standing function improves the reach and accessibility available to the user. #### VII. PERFORMANCE DATA । The following performance data has been provided in support of the substantial equivalence determination. ## Biocompatibility Testing - Bio-Compatibility testing requirements were evaluated for all potential body (skin) contacting O materials. Cytotoxicity testing was performed per 'ISO 10993 Part 5: Testing for in vitro cytotoxicity', and Dermal Sensitization testing and/or Primary Skin Irritation testing was performed per 'ISO 10993 Par10: Tests for irritation and skin sensitization'. Testing was conducted on all body contact materials on the MPSS, including: Meshtex fabric, Startex fabric, Spacetex 4000U™ fabric, O-Vinyl fabric, Style 6499 Polyester fabric, Self-Skinning Skin PU Foam (Bolasto F380 (RN7548)). #### l Software Verification and Validation Testing - o Software verification and validation testing have been conducted and documentation is provided as recommended by FDA's Guidance for Industry and FDA Staff, "Guidance for the Content of Premarket Submissions for Software Contained in Medical Devices." The software for this device is considered to have a "Moderate level of Concern" because "prior to mitigation of hazards, a failure of the Software Device could result in Minor Injury, either to a patient or to a user of the device." - -Electrical Safety and electromagnetic compatibility (EMC) {6}------------------------------------------------ 510(k) Summary Modular Power Standing System - o Electromagnetic Compatibility testing has been conducted on the Modular Power Standing System. The system complies with ISO 7176-21, Requirements and Test Methods for Electromagnetic Compatibility of Electrically Powered Wheelchairs and Scooters. ### -Mechanical and acoustic testing - Mechanical testing of the Modular Power Standing System was carried out to cover functional o verification and device performance. Testing established correct functionality according to the relevant ISO 7176 standards. No acoustic testing was required to demonstrate device safety and effectiveness of the subject device. । Animal Study - o Animal performance testing was not required to demonstrate the safety and effectiveness of the subject device. - -Clinical Studies - Clinical testing was not required to demonstrate the safety and effectiveness of the subject device. o The following table provides a comparison of technological characteristics with the predicate device (Levo X3) and the reference device (Modular Power Positioning System) to demonstrate substantial equivalence. | | Subject Device | Predicate (A) | Reference device (B) | | |-----------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | | Motion Concepts Modular<br>Power Standing System | Levo C3 | Motion Concepts Modular<br>Power Positioning System | Comparison | | 510k number | N/A | K083017 | K150574 | N/A | | Product Code | IPL 890.3900 | IPL 890.3900 | ITI 890.3860 | The subject device<br>is identical to (A) | | Indications for<br>Use | The Modular Power Standing<br>System is appropriate for use by<br>individuals who drive a power<br>wheelchair and cannot stand up<br>on their own. The Modular<br>Power Standing System allows<br>such users to change position<br>including from seating to<br>standing, standing to seating, or<br>any position in between. The<br>device is appropriate for indoor<br>and outdoor use. Motion<br>Concepts makes no claims as to<br>the therapeutic effectiveness of<br>the products. Our only claims<br>relate to the ability of the<br>products to provide safe and<br>reliable powered repositioning<br>on the equipment onto which<br>they are installed. | The LEVO C3 power<br>wheelchair with optional<br>seating and standing position<br>function may be of interest<br>for any individuals who<br>needs a power wheelchair<br>and cannot stand up on their<br>own such as people with<br>spinal cord injury, spina<br>bifida, cerebral palsy,<br>multiple sclerosis, muscular<br>dystrophy, polio,<br>rheumatism, etc | N/A | The subject device<br>is equivalent to (A). | | | Subject Device<br>Motion Concepts Modular<br>Power Standing System | Predicate (A)<br>Levo C3 | Reference device (B)<br>Motion Concepts Modular<br>Power Positioning System | | | Picture (in<br>standing mode) | | | N/A | The subject device<br>is equivalent to (A)<br>for standing<br>function. | | Picture (in<br>tilt/recline/eleva<br>te mode) | | | | The subject device<br>is equivalent to (B)<br>for tilt, recline, and<br>elevate functions. | | Target<br>Population | Paraplegics or quadriplegics<br>People with spinal cord<br>injury, spina bifida, cerebral<br>palsy, multiple sclerosis,<br>muscular dystrophy, polio,<br>rheumatism, and other<br>diseases and conditions<br>which cause the individual<br>to require a power<br>wheelchair and not be able<br>to shift his/her weight | The LEVO C3 power<br>wheelchair with optional<br>seating and standing position<br>function may be of interest<br>for any individuals who<br>needs a power wheelchair<br>and cannot stand up on their<br>own such as people with<br>spinal cord injury, spina<br>bifida, cerebral palsy,<br>multiple sclerosis, muscular<br>dystrophy, polio,<br>rheumatism, etc.. | Quadriplegics<br>persons with ALS, MS,<br>spinal muscular<br>atrophy, and any other<br>disability which causes<br>the individual to<br>require a power<br>wheelchair and not be<br>able shift his/her<br>weight | The subject device<br>is equivalent to (A). | | Design | Link based mechanisms<br>powered by electro-mechanical<br>linear actuators | Link based mechanisms<br>powered by electro-<br>mechanical linear actuators | Link based mechanisms<br>powered by electro-<br>mechanical linear actuators | The subject device<br>is equivalent to (A)<br>and (B). | | Materials | steel tube and plate, aluminum,<br>powder-coated | steel tube and plate,<br>aluminum, powder-coated | steel tube and plate,<br>aluminum, powder-coated | The subject device<br>is equivalent to (A)<br>and (B). | | Weight Capacity | 250 lbs | 310 lbs | 300 lbs (250lbs with<br>elevate) | The subject device<br>is equivalent to (B)<br>with elevate. | | Performance -<br>Tilt | 45° | 35° | 50° | The subject is<br>functionally<br>equivalent to (A)<br>and (B) | | Performance -<br>Recline | 178° | Info Not available | 168° | The subject device<br>is functionally<br>equivalent to (A)<br>and (B). It is noted<br>that the slight | | | Subject Device<br>Motion Concepts Modular<br>Power Standing System | Predicate (A)<br>Levo C3 | Reference device (B)<br>Motion Concepts Modular<br>Power Positioning System | Comparison | | Performance –<br>Elevation | 6.5" | N/A | 12" | increase in<br>maximum amount<br>of recline compared<br>to (B) is required to<br>provide an effective<br>stand option<br>The subject device<br>has less elevation<br>than (B), This is<br>offset by the stand<br>feature which offers<br>alternatives for<br>comfort, positioning<br>and versatility. | | Seat width range | 16 to 21 inches | 12.5 to 20.5 inches | 15 to 24 inches | The subject device<br>has smaller width<br>range than (A) or (B) | | Seat depth range | 16 to 20 inches | 13.75 to 25 inches | 15 to 22 inches | The subject device<br>has smaller depth<br>range than (A) or (B) | | Back height<br>range | 20 to 28 inches | 12 to 21.5" | 18 to 30 inches | The subject device<br>has smaller back<br>height range than<br>(B) | | Mechanical<br>Safety | - wheelchair remains stable<br>when fully tilted, reclined<br>seat, elevated, standing<br>speed is reduced when<br>patient is positioned<br>beyond pre-set limits.<br>- drive lock-out prevents user<br>from driving power chair<br>while tilted beyond a pre-<br>set limits<br>- tilt limit is available<br>- Front caster lock to reduce<br>risk of tipping forward while<br>in stand-up position | - The speed is reduced to<br>half speed as soon as<br>the patient is not in the<br>sitting position | - wheelchair remains<br>stable with fully<br>elevated, tilted, and<br>reclined seat - center-<br>of-gravity shift further<br>enhances stability<br>- drive lock-out prevents<br>user from driving<br>power chair while tilted<br>beyond a pre-set limit<br>speed is reduced when<br>patient is positioned<br>beyond pre-set limits.<br>- tilt limit is available | The subject device<br>includes safety<br>features equivalent<br>to those listed for<br>both (A) and (B) | | Where Used | - private residences<br>- chronic-care facilities<br>- indoors, outdoors | The product provides high<br>indoor and outdoor mobility<br>on surfaces like tar, grass<br>and gravel | - private residences<br>chronic-care facilities<br>indoors, outdoors<br>- | The subject device<br>is equivalent to (A)<br>and (B). | | Electrical Safety | - electrical components are<br>24 volts maximum<br>current limit built into relay<br>box | Info Not available | - electrical components<br>are 24 volts maximum<br>current limit built into<br>relay box | Identical to (B) | | Energy Used | 24 VDC Wheelchair Batteries | 24 VDC Wheelchair Batteries | 24 VDC Wheelchair<br>Batteries | Identical to (A) and<br>(B). | | | Subject Device | Predicate (A) | Reference device (B) | | | | Motion Concepts Modular | Levo C3 | Motion Concepts Modular | Comparison | | | Power Standing System | | Power Positioning System | | | Power stand-up<br>feature | Chest support and knee support<br>standard | Chest support and knee<br>support standard | Not Applicable | The subject device<br>is equivalent to (A) | | Motor Type | Linear actuator,<br>Gear reduction screw type | Info Not available | Linear actuator,<br>Gear reduction screw type | Identical to (B) | | Motor Voltage | 24VDC | Info Not available | 24VDC | Identical to (B) | | Motor Maximum<br>Current | 4 Amps | Info Not available | 4 Amps | Identical to (B) | | Power | 96W | Info Not available | 96W | Identical to (B) | | Standards Met | ISO 7176 see details below | ISO 7176<br>ANSI/RESNA | RESNA WC-1:2009<br>RESNA WC-2:2009 | The subject device<br>is equivalent to (A)<br>and (B). | {7}------------------------------------------------ Page 5 of 8 510(k) Summary Modular Power Standing System Motion opts {8}------------------------------------------------ Motion opts # 510(k) Summary Modular Power Standing System {9}------------------------------------------------ Motion # 510(k) Summary Modular Power Standing System ## Standards Met | Standard | Description | FDA Recognition<br>Number | |------------------|------------------------------------------------------------------------------------------------------------------------------------|---------------------------| | ISO 7176-1:2014 | Wheelchairs - Part 1: Determination of static stability | 16-195 | | ISO 7176-2:2017 | Wheelchairs - Part 2: Determination of dynamic stability of electrically powered wheelchairs | 16-202 | | ISO 7176-3:2012 | Wheelchairs - Part 3: Determination of effectiveness of brakes | 16-192 | | ISO 7176-4:2008 | Wheelchairs - Part 4: Energy consumption of electric wheelchairs and scooters for determination of theoretical distance range | 16-162 | | ISO 7176-5:2008 | Wheelchairs - Part 5: Determination of dimensions, mass and maneuvering space | 16-163 | | ISO 7176-6:2018 | Wheelchairs - Part 6: Determination of maximum speed of electrically powered wheelchairs | 16-204 | | ISO 7176-7:1998 | Wheelchairs - Part 7: Measurements of seating and wheel dimensions | 16-196 | | ISO 7176-8:2014 | Wheelchairs - Part 8: Requirements and test methods for static, impact and fatigue strengths | 16-197 | | ISO 7176-9:2009 | Wheelchairs - Part 9: Climatic tests for electric wheelchairs | 16-167 | | ISO 7176-10:2008 | Wheelchairs - Part 10: Determination of obstacle-climbing ability of electrically powered wheelchairs | 16-164 | | ISO 7176-11:2012 | Wheelchairs - Part 11: Test dummies | 16-190 | | ISO 7176-13:1989 | Wheelchairs - Part 13: Determination of coefficient of friction of test surfaces | 16-25 | | ISO 7176-14:2008 | Wheelchairs - Part 14: Power and control systems for electrically powered wheelchairs and scooters - Requirements and test methods | 16-165 | {10}------------------------------------------------ Page 8 of 8 MotionConcepts ## 510(k) Summary Modular Power Standing System | Standard | Description | FDA Recognition<br>Number | |-------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------| | ISO 7176-15:1996 | Wheelchairs – Part 15: Requirements for information disclosure, documentation and<br>labelling | 16-27 | | ISO 7176-16:2012 | Wheelchairs – Part 16: Resistance to ignition of postural support devices | 16-191 | | ISO 7176-21:2009 | Wheelchairs – Part 21: Requirements and test methods for electromagnetic compatibility<br>of electrically powered wheelchairs and scooters, and battery chargers | 16-166 | | ISO 7176-22:2014 | Wheelchairs – Part 22: Set-up procedures | 16-198 | | ISO 7176-30:2018 | Wheelchairs – Part 30: Wheelchairs for changing occupant posture – Test methods and<br>requirements | N/A | | ISO 10993-5:2009 | Part 5: Biological Evaluation of Medical Devices – Tests For In Vitro Cytotoxicity | 2-245 | | ISO 10993-10:2010 | Part 10: Biological Evaluation of Medical Devices – Tests for irritation and skin sensitization | 2-174 | | EN 1021-1/-2:2014 | Testing of Ignitability For Upholstered Furniture…
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