Merits Model R106/R136 Rehab Wheelchair

K170517 · Merits Healthcare Industries (Suzhou) Co., Ltd. · IOR · Nov 16, 2017 · Physical Medicine

Device Facts

Record IDK170517
Device NameMerits Model R106/R136 Rehab Wheelchair
ApplicantMerits Healthcare Industries (Suzhou) Co., Ltd.
Product CodeIOR · Physical Medicine
Decision DateNov 16, 2017
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 890.3850
Device ClassClass 1

Intended Use

The Merits Model R106/R136 Rehab Wheelchair is to provide mobility to persons limited to a sitting position.

Device Story

Manual wheelchairs (R106/R136) providing mobility for users limited to sitting position. Features include adjustable headrest, armrests, and seat dimensions; reclining backrest (9° to 57°); tilt-in-space seat (4° to 34°); and shear reduction system aligning user pivot points with backrest recline to minimize sliding and pressure. Operated by user or attendant in indoor/outdoor environments on dry, level surfaces. Steel frame construction; manual wheel locks for safety. Provides mobility and postural support; shear reduction system improves comfort and reduces skin pressure during recline.

Clinical Evidence

Bench testing only. Compliance with ISO 7176 series (stability, brakes, dimensions, strength, friction, labeling, ignition resistance) and ISO 10993 (cytotoxicity, irritation, sensitization) demonstrated performance equivalent to predicate.

Technological Characteristics

Manual wheelchair; steel frame; polyurethane (PU) foam seating; PU tires. Adjustable headrest, armrests, and seat dimensions. Shear reduction system via pivot point alignment. ISO 7176-16:2012 compliant upholstery. No electronic components or software.

Indications for Use

Indicated for persons limited to a sitting position requiring mobility assistance.

Regulatory Classification

Identification

A mechanical wheelchair is a manually operated device with wheels that is intended for medical purposes to provide mobility to persons restricted to a sitting position.

Predicate Devices

Related Devices

Submission Summary (Full Text)

{0}------------------------------------------------ Image /page/0/Picture/0 description: The image shows the logos of the Department of Health & Human Services and the U.S. Food & Drug Administration (FDA). The Department of Health & Human Services logo is on the left, and the FDA logo is on the right. The FDA logo includes the letters "FDA" in a blue square, followed by the words "U.S. Food & Drug Administration" in blue text. The word "Administration" is on the second line. November 16, 2017 Merits Healthcare Industries (suzhou) Co., Ltd. Guangyong Li Manager No.29, Fuzhou Road Taicang City, 215411 CN Re: K170517 Trade/Device Name: Merits Model R106/R136 Rehab Wheelchair Regulation Number: 21 CFR 890.3850 Regulation Name: Mechanical Wheelchair Regulatory Class: Class I Product Code: IOR Dated: September 29, 2017 Received: October 19, 2017 Dear Guangyong Li: 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. 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 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); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); {1}------------------------------------------------ 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 http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance. For comprehensive regulatory information about mediation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/) and CDRH Learn (http://www.fda.gov/Training/CDRHLearn). 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 (http://www.fda.gov/DICE) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100). Sincerely, # Michaelリ. Hoffmann -S Carlos L. Peña. PhD. MS for Director Division of Neurological and Physical Medicine Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ # Indications for Use 510(k) Number (if known) K170517 #### Device Name Merits Model R106/R136 Rehab Wheelchair #### Indications for Use (Describe) The Merits Model R106/R136 Rehab Wheelchair is to provide mobility to persons limited to a sitting position. 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}------------------------------------------------ # 510(k) SUMMARY #### Merits Healthcare Industries. (suzhou) Co., LTD. 510(k) Premarket Notification K170517 #### Submitter: Merits Healthcare Industries. (suzhou) Co., LTD. No.29, Fuzhou Road, Taicang City. Jiangsu province, China. ## Contact Person: Guangyong Li Merits Healthcare Industries. (suzhou) Co., LTD. No.29, Fuzhou Road, Taicang City. Jiangsu province, China. Phone: +86-512-53510000 ext.211 Fax: +86-512-82775985 ### Date Prepared: November 15, 2017 ## Proprietary Name: Merits Model R106/R136 Rehab Wheelchair ### Common name: Manual Wheelchair ### Classification name: Wheelchair, Mechanical ## Product Code: IOR ### Indications for Use The Merits Model R106/R136 Rehab Wheelchair is to provide mobility to persons limited to a sitting position. {4}------------------------------------------------ # The Predicate Device: This submission indicates the Substantial Equivalence of the Merits Model R106/R136 Rehab Wheelchair, with the predicate ORION II (Heavy Duty 350lbs and 500lbs) mechanical wheelchair (K101277). R106/R136 has the same intended uses and similar indications, technological characteristics and principles of operation with predicate device. # Device Description The Merits Model R106/R136 Rehab Wheelchair are manual wheelchairs. They have adjustable headrest, adjustable armrests, cozy ergonomics seat and multiple axle position. The seat and back are supported by two cylinders, so the fully back reclines can be adjusted from 9° to 57° and seat tilting angles from 4° to 34° . The casters are 7"*1" PU wheels with height adjustable forks and the rear wheels are 24"*1-3/8" polyurethane spoke wheels (R106) or 12-1/2"*2-1/4" polyurethane spoke wheels (R136). The wheelchair also has a shear reduction system: by carefully aligning the pivot points of the user and the Recline Backrest of the wheelchair, to minimize the sliding down of the user and also minimize the shear force and pressure against the back. The armrest height can be adjusted from 8" to 12". Its seat width is also adjustable: 16" /17" /18" /19" and 20" and seat depth: 18" /19" and 20". The upholstery of the device complies with ISO 7176-16:2012 Resistance to ignition of postural support devices. The device can be operated indoors, or outdoors on dry, level surfaces composed of concrete, blacktop, or asphalt under normal driving conditions. {5}------------------------------------------------ # Discussions of Non-clinical Tests Performed for Determinations of Substantial equivalence are as follows: | ISO 7176-1:2014 | Determination of Static Stability | |-------------------|----------------------------------------------------------------------------------------------------| | ISO 7176-3:2012 | Determination of effectiveness of brakes | | ISO 7176-5:2008 | Determination of overall dimensions, mass and maneuvering<br>space | | ISO 7176-7:1998 | Method of Measurement of Seating and Wheel Dimensions | | ISO 7176-8:2014 | Requirements and test methods for static, impact and fatigue<br>strengths | | ISO 7176-11:2012 | Test dummies | | ISO 7176-13:1989 | Determination of coefficient of friction of test surfaces | | ISO 7176-15:1996 | Requirements for Information Disclosure, Documentation and<br>Labeling | | ISO 7176-16:2012 | Resistance to ignition of postural support devices | | ISO 14971:2007 | Medical devices -- Application of risk management to medical<br>devices | | ISO 10993-5:2009 | Biological evaluation of medical devices - Part 5: Tests for in<br>vitro cytotoxicity | | ISO 10993-10:2010 | Biological evaluation of medical devices - Part 10: Tests for<br>irritation and skin sensitization | The results of the testing confirm that the device meets specifications and is substantially equivalent to the predicate device. {6}------------------------------------------------ # Comparison of the Technological Characteristics: The Merits Model R106/R136 Rehab Wheelchair, is substantially equivalent to the ORION II (Heavy Duty 350lbs and 500lbs) mechanical wheelchair (K101277). Both products are mechanical designed for use as personal manual mobility aids. Performance characteristics and drive mechanisms are similar and all have the same intended function and use which is to provide mobility to persons limited to a sitting position. Additional, they are all constructed from the same basic materials, have the same basic operational principles or operated by others. The comparison table is as follow: | Characteristics | | The Merits Model<br>R106 Rehab<br>Wheelchair | The Merits Model<br>R136 Rehab<br>Wheelchair | ORION II (Heavy Duty<br>350lbs and 500lbs)<br>mechanical<br>wheelchair (K101277) | |-----------------------------------|--------|---------------------------------------------------------------------|---------------------------------------------------------------------|----------------------------------------------------------------------------------| | Indications for Use | | To provide mobility to<br>persons limited to a<br>sitting position. | To provide mobility to<br>persons limited to a<br>sitting position. | To provide mobility to<br>persons limited to a<br>sitting position. | | Dimension | Length | 47.5" (±1") | 44.5(±1") | 47" | | | Width | 28-32" (±1") | 26"-30" (±1") | 24.5-33.5" | | | Height | 42" (±1") | 42" (±1") | 42" | | Weight | Total | 89 lbs | 62 lbs | 65 lbs | | Weight Capacity | | 300 lbs | 300 lbs | 350 lbs | | Seat width | | 16-20" | 16-20" | 15-24" | | Seat height | | 19-21" | 21" | 16-20" | | Seat depth | | 18-20" | 18-20" | 15-24" | | Tires | | Front: 7"/ Rear: 24" | Front: 7"/ Rear: 12-1/2" | Front: 4",5",6",7",8"/<br>Rear: 12",20",22",24" | | Headrest | | Adjustable | Adjustable | Adjustable | | Armrest | | Height Adjustable<br>(8"~12") | Height Adjustable<br>(8"~12") | Height Adjustable<br>(9-1/2"~14") | | Back Recline | | 9°~57° | 9°~57° | 6°~36°(Optional) | | Seat Tilt | | 4°~34° | 4°~34° | 3°~48° | | Elevating Legrest | | Standard | Standard | Optional | | Seat/Backrest Pad | | Cozy Ergonomics PU<br>Foam | Cozy Ergonomics PU<br>Foam | Cozy Ergonomics PU<br>Foam | | Rear Axle Position | | Multiple | Fixed | Multiple | | Shear Reduction | | Aligned Backrest<br>Recline & User Pivot<br>Points | Aligned Backrest<br>Recline & User Pivot<br>Points | None | | Hand Brake<br>(Brake Force/Dist.) | | 13.5N/0.5M | 13.5N/0.5M | 13.5N/0.5M | | Frame Construction | | Fixed Frame<br>(Not foldable) | Fixed Frame<br>(Not foldable) | Fixed Frame<br>(Not foldable) | | Frame Material | | Steel | Steel | Steel | | Turning Radius | | 30"~35.8"<br>(76.5cm~91cm) | 32"~38.1"<br>(81.5cm~96.8cm) | 28"~37"<br>(71cm~94cm) | | Safety Feature | | Manual Wheel Lock | Manual Wheel Lock | Manual Wheel Lock | {7}------------------------------------------------ The comparison of the technical details between R106/R136 and its predicate device are summarized in the following: - a. Dimension: The dimensions of our device and the predicate are similar. And our device has passed ISO 7176-1:2014 (Determination of Static Stability) and ISO 7176-2:2001(Determination of Dynamic Stability of electric wheelchairs). So there is no deleterious affection of safety and effectiveness about the difference on Dimension with predicated device. - b. Weight: Although the total weight of R106/R136 is heavier than ORION II (Heavy Duty 350lbs and 500lbs) mechanical wheelchair (K101277). The device has passed ISO 7176-8 (Requirements and test methods for static, impact and fatigue strengths) test (Please see Appendix IV: Test reports). So there is no deleterious affection of safety and effectiveness about the difference on Weight with predicate device. - c. Cozy Ergonomics Seating System: Both of our devices and the predicate are equipped with similar Cozy Ergonomics PU foam Seat/Backrest Pad, adjustable Headrest and Armrest which can offer the most comfortable seating experiences to users. Our R106/R136 is supplied with a standard Elevating Legrest, while the predicated device is provided it as an option. The Elevating Legrest can provide better strain-relief for legs. - d. Multiple Rear Axle Position: Both our R106 and the predicate device are provided with Multiple Rear Axle Positions to allow users to change its seat height to a best fitting position. But for the attendant control wheelchair, the seat height adjustment is not as important as the stability, so a Fixed Rear Axle Position is used on our R136 device to achieve the most stable position. - e. Shear Reduction: On the predicated device, the Reclined Backrest and user pivot points are not aligned resulting in a non-synchronized movement. As a result, when it reclines, the headrest and back support move up, forcing the user to slide down the chair to compensate. This leads to shear and friction forces. Our R106/R136 devices are carefully designed to align the pivot points of the user and the Recline Backrest of the wheelchair. This minimizes the sliding down of the user while reclining the backrest. And this also minimizes the shear force and pressure against the back. - f. Frame Construction and material: Both of our devices and the predicated device are the same steel, fixed frames. - g. Safety Feature: Both of our devices and the predicated device are equipped with Manual Wheel Locks to prevent unexpected movement while parking. The minor differences between R106/R136 and its predicate device raise no new issues of safety or effectiveness. Performance data demonstrate that the R106/R136 is safe. {8}------------------------------------------------ # Conclusions According to comparison table, the differences on weight capacity, adjustable back angle, adjustable armrest height and dimensions do not deleteriously affect the safety and effectiveness of the device. The non-clinical testing and the predicate comparisons demonstrate that any differences in their technological characteristics do no raise any new questions of safety or effectiveness. So based on the design, performance specifications and testing and intended use, The Merits Model R106/R136 Rehab Wheelchair, is substantially equivalent to the ORION II (Heavy Duty 350lbs and 500lbs) mechanical wheelchair (K101277).
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