Life Spine Foot and Ankle Plating System
K-Number: K172973 · 2017-12-21
Device Summary
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.
Related Clinical Trials
Other Devices by Life Spine, Inc.
Related Devices (Code: HRS)
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.