Advanced Back Technologies
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Advanced Back Technologies is a medical device manufacturer, with 3 devices listed in FDA 510(k) and FDA GUDID (FDA Class II) and 2 FDA recalls as of 13 Nov 2026.
- Devices
- 3
- FDA recalls
- 2
Registry facts
- Registries
- FDA 510(k) 2
- FDA GUDID 1
- Device classes
- FDA Class II 3
- FDA recalls
At a glance
Market reach
- United States
- FDA recalls
What Advanced Back Technologies makes
Advanced Back Technologies manufactures programmable powered traction systems designed for spinal decompression and disc space distraction, including models like the Extentrac Elite and EXTENTRAC.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance and UDI registration.
Catalogue
- Regimes: 510(k) Registry: GUDID
Extentrac Elite Ref K031996
Regimes: 510(k) Registry: 510(k)Extentrac Ref K980021
Regimes: 510(k) Registry: 510(k)
FDA recalls
FDA recall records list 2 recalls initiated by Advanced Back Technologies, initiated on 2015-05-13. By recorded status: 2 terminated. The reasons filed fall into these groups: other reasons as filed. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
2015
- 13 May 2015 Z-1717-2015 Class II Terminated Item is marketed for use in patients weighing up to 350 lbs, but the device was only approved for use in patients up to 300 lbs
Full distribution text
- 13 May 2015 Z-1718-2015 Class II Terminated Item is marketed for use in patients weighing up to 350 lbs, but the device was only approved for use in patients up to 300 lbs
Full distribution text
- 13 May 2015 Z-1717-2015 Class II Terminated Item is marketed for use in patients weighing up to 350 lbs, but the device was only approved for use in patients up to 300 lbs
Frequently asked questions
How many devices does Advanced Back Technologies have in the registry?
The registry currently lists 3 devices for Advanced Back Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Advanced Back Technologies's devices?
Among its 3 most recently registered devices, Advanced Back Technologies has devices listed in FDA 510(k) (2 devices) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Advanced Back Technologies's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Advanced Back Technologies's devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Advanced Back Technologies?
FDA recall records list 2 recalls initiated by Advanced Back Technologies, the most recent initiated on 13 May 2015. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Advanced Back Technologies in the registry?
The most recently registered devices listed for Advanced Back Technologies include Extentrac Elite M100, EXTENTRAC ELITE and EXTENTRAC.