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FDA 510(k)

Hammertoe Truss System (HTS)

K-Number: K221283 · 2022-09-06

Applicant4Web Medical, Inc.
Decision Date2022-09-06
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Hammertoe Truss System (HTS) is a medical device manufactured by 4Web Medical, Inc.. It received FDA 510(k) clearance on 2022-09-06 under approval number K221283. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Hammertoe Truss System (HTS)?

Hammertoe Truss System (HTS) is a medical device that received FDA 510(k) clearance on 2022-09-06. It is manufactured by 4Web Medical, Inc.. The 510(k) number is K221283.

When was Hammertoe Truss System (HTS) approved by the FDA?

Hammertoe Truss System (HTS) received FDA 510(k) clearance on 2022-09-06, under approval number K221283.

What company makes Hammertoe Truss System (HTS)?

Hammertoe Truss System (HTS) is manufactured by 4Web Medical, Inc..

What is the FDA product code for Hammertoe Truss System (HTS)?

The FDA product code for Hammertoe Truss System (HTS) is HTY.

Other Devices by 4Web Medical, Inc.

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Related Devices (Code: HTY)

K161489Syntorr K-wire and Pin SystemSyntorr, Inc. K160264Additive Orthopaedics Hammertoe Correction SystemAdditive Orthopaedics, LLC K160194StarFuse Interphalangeal PinPhalanx Innovations K152662S-WireSpinal Resources, Inc. K153204In2Bones Kirschner wireIn2bones Sas K152627IFS Fixation Scaffold SystemMetric Medical Devices, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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