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FDA 510(k)

Life Spine Foot and Ankle Plating System

K-Number: K172973 · 2017-12-21

Decision Date2017-12-21
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Life Spine Foot and Ankle Plating System is a medical device manufactured by Life Spine, Inc.. It received FDA 510(k) clearance on 2017-12-21 under approval number K172973. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Life Spine Foot and Ankle Plating System?

Life Spine Foot and Ankle Plating System is a medical device that received FDA 510(k) clearance on 2017-12-21. It is manufactured by Life Spine, Inc.. The 510(k) number is K172973.

When was Life Spine Foot and Ankle Plating System approved by the FDA?

Life Spine Foot and Ankle Plating System received FDA 510(k) clearance on 2017-12-21, under approval number K172973.

What company makes Life Spine Foot and Ankle Plating System?

Life Spine Foot and Ankle Plating System is manufactured by Life Spine, Inc..

What is the FDA product code for Life Spine Foot and Ankle Plating System?

The FDA product code for Life Spine Foot and Ankle Plating System is HRS.

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Official Source

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