510(k) · Cleared
ClearedZ10 Wheelchair Push and Brake Assist Device
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Otto Bock Healthcare LP · ITI Wheelchair, Powered
Cleared on Sep 16, 2011 as substantially equivalent to K073701 (Dane Technologies, 2008) after a 134-day review. Its family tree reaches back 6 generations to 1990.
- Decided
- Sep 16, 2011
- Review
- 134 days
- Class
- Class II
- Product code
- ITI
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 6 generations to K900565 (1990). 7 ancestors in all. No later device cites it as a predicate yet.
- Root · 6 generations backK900565 Invacare Power 9000 Series WheelchairInvacare Corp. · 1990
- 5 generations backK982064 Action Storm Ranger II, Action Storm Power 9000Invacare Corp. · 1998
- 4 generations backK991168 Arrow FWD Power WheelchairInvacare Corp. · 1999 · Recalled
- 3 generations backK012909 Xterra GT Power WheelchairInvacare Corp. · 2001
- 2 generations backK023589 Storm TDX Power WheelchairInvacare Corp. · 2002 · Recalled
- 1 generation backK073701 Dane Technologies Wheelchair Mover, Model WM 2000Dane Technologies · 2008
- This deviceK111278 Z10 Wheelchair Push and Brake Assist DeviceOtto Bock Healthcare LP · 2011
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K900565 | Invacare Power 9000 Series Wheelchair | Invacare Corp. | 1990 | — |
| −5 | K982064 | Action Storm Ranger II, Action Storm Power 9000 | Invacare Corp. | 1998 | — |
| −4 | K991168 | Arrow FWD Power Wheelchair | Invacare Corp. | 1999 | 2 |
| −3 | K012909 | Xterra GT Power Wheelchair | Invacare Corp. | 2001 | — |
| −2 | K023589 | Storm TDX Power Wheelchair | Invacare Corp. | 2002 | 7 |
| −1 | K073701 | Dane Technologies Wheelchair Mover, Model WM 2000 | Dane Technologies | 2008 | — |
| 0 (this device) | K111278 | Z10 Wheelchair Push and Brake Assist Device | Otto Bock Healthcare LP | 2011 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1997 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in ITI? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new ITI device
- #1 K220747 Power Wheelchair (N5515B)score 40.2 · 4 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (1)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K073701 | Dane Technologies Wheelchair Mover, Model WM 2000Summary page 1…edicate Device 1. Name: Dane Technologies Wheelchair Mover 2. Manufacture: Dane Technologies 3. K Number: K073701 4. Date Cleared: January 8, 2008 D. Description of the Device The z1 0 is a powerful push and brake assi… | 2008 |
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 21 years and passes through 3 companies; a new generation was cleared every 3.6 years on median.
- 2 of the 7 ancestors have a recall of any class.
How does its category compare?
All ITI devicesITI Wheelchair, Powered: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.
FDA decisions per year · ITI
29in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · ITI
90in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · ITI
13so far in 2026, the most since 2007
Class I (2 since 2007) Class II/III not classified
Adverse event reports per year · ITI
647in 2025
MAUDE reports naming product code ITI, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 18 | 42 | 3 | 123 |
| 2008 | 9 | 49 | 3 | 133 |
| 2009 | 7 | 63 | 1 | 183 |
| 2010 | 6 | 46 | 2 | 157 |
| 2011 | 4 | 101 | 0 | 525 |
| 2012 | 6 | 155 | 1 | 2,919 |
| 2013 | 5 | 177 | 0 | 8,741 |
| 2014 | 5 | 213 | 0 | 7,282 |
| 2015 | 10 | 174 | 0 | 4,685 |
| 2016 | 6 | 173 | 1 | 1,575 |
| 2017 | 4 | 159 | 2 | 301 |
| 2018 | 4 | 117 | 0 | 273 |
| 2019 | 3 | 244 | 0 | 264 |
| 2020 | 6 | 278 | 0 | 205 |
| 2021 | 13 | 209 | 3 | 166 |
| 2022 | 16 | 96 | 0 | 135 |
| 2023 | 8 | 128 | 0 | 223 |
| 2024 | 38 | 125 | 1 | 146 |
| 2025 | 29 | 90 | 3 (2) | 647 |
| 2026 | 36 | 108 | 13 | — |
What is it indicated for?
Provide mobility to persons physically challenged and limited to sitting positions due to:
* Paisies/Paralyses
* Loss of limbs
* Defective and/or deformed limbs
* Joint contractures
* Joint defects
* Other diseases
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K111278 · printed Nov 6, 2026
Cite this page
510(k) Report. “K111278: Z10 Wheelchair Push and Brake Assist Device.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K111278
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026