510(k) · Cleared
ClearedAlphatrac, Model A200
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Teftec Corp. · ITI Wheelchair, Powered
Cleared on Nov 6, 1998 after an 87-day review. FDA’s file for it is a 510(k) statement, which names no predicate.
- Decided
- Nov 6, 1998
- Review
- 87 days
- Class
- Class II
- Product code
- ITI
- Recalls
- None
- Predicates
- 0
FDA’s file for it is a 510(k) statement, which names no predicate.
Sources: FDA 510(k) database (decision fields), the FDA 510(k) statement (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?
FDA’s file for it is a 510(k) statement, which names no predicate.
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.
How does its category compare?
All ITI devicesITI Wheelchair, Powered: FDA decisions, review times, recalls and adverse event reports over 20 years.
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?
Indications for use for the Alpha Trac powered wheelchair base: Alpha Trac design definitions and functional parameters are indicated for usage for anyone with limited mobility due to weak, amputated or non-functional extremities or improper, unsafe or non-existent gaxt patterns. Also due to the specific driving control supplied by the TransAxle persons with spasticity or ataxic movements in their extremity’s that are not candidates for other types of…
Read the full statement (223 words)
Indications for use for the Alpha Trac powered wheelchair base:
Alpha Trac design definitions and functional parameters are indicated for usage for anyone with limited mobility due to weak, amputated or non-functional extremities or improper, unsafe or non-existent gaxt patterns. Also due to the specific driving control supplied by the TransAxle persons with spasticity or ataxic movements in their extremity’s that are not candidates for other types of mobility without extensive modification may be appropriate for the AlphaTrac with no modifications.
This usage would be indicated but not limited to the following types of injury’s:
Spinal Cord Injury (SCI)
Head Injury (CHI)
Muscular Dystrophy (MD)
Cerebral Palsy (CP)
Parkinson’s
Amputees
Brown Sequard’s Syndrome and resultant paralysis
Severe Arthritics (RA) (OA)
Multiple Sclerosis (MS)
Amyotrophic Lateral Sclerosis (ALS)
Huntington’s Corea
Traumatic Brain Injury (TBI)
Anoxic Encephalopathy .
Anoxia .
Guillain-Barre Syndrome
Quadriplegia
Paraplegia
Hemiplegia
Tetraplegia .
Proximal weakness
Quadriparesis
Paraparesis
Cercutad vascutal Acuiiiviii (U v A OF JUIFOKE)
This is not meant to be an all inclusive list, anyone needing power assistance with their mobility may be an appropriate client for an AlphaTrac powered wheelchair. This would usually be decided by clinical evaluation of the client’s strength, sitting balance, mobility needs, size constraints and driving capability at their local rehab facility.
If you have an further questions please feel free to contact us directly.
Indications for use read by OCR from a scanned FDA 510(k) statement, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K982815 · printed Nov 5, 2026
Cite this page
510(k) Report. “K982815: Alphatrac, Model A200.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K982815
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Page last updated Nov 3, 2026