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510(k) Data Aggregation
(148 days)
The Life Spine Subtalar Implant System
The LIFE SPINE Subtalar implant is indicated for use in the treatment of the hyperpronated foot and stabilization of the subtalar joint. It is designed to block forward, downward and medial displacement of the talus, thus allowing normal subtalar joint motion but blocking excessive pronation and the resulting sequela.
The LIFE SPINE Subtalar implants are intended for single use only.
The LIFE SPINE Subtalar Implant System is a one piece titanium implant for treating hyperpronation of the foot. The system includes instruments (trial sizers, k-wires, and driver) to facilitate placement of the implant. Implants are manufactured from titanium alloy (Ti 6Al-4V ELI).
All implants are intended for single use only and should not be reused under any circumstances. Do not use any of the Subtalar Implant System components with components from any other system or manufacturer. The Subtalar Implant System components should never be reused under any circumstances.
This document is a 510(k) premarket notification for a medical device called "The LIFE SPINE Subtalar Implant System". It describes the device, its intended use, and claims substantial equivalence to predicate devices. However, it does not contain any information about acceptance criteria or a study proving that the device meets acceptance criteria.
The document primarily focuses on regulatory approval based on substantial equivalence, which often relies on demonstrating that a new device is as safe and effective as a legally marketed predicate device, rather than requiring extensive performance studies against specific acceptance criteria.
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