Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Life Spine ALIF Buttress Plate System

K-Number: K222628 · 2022-11-16

Decision Date2022-11-16
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Life Spine ALIF Buttress Plate System is a medical device manufactured by Life Spine, Inc.. It received FDA 510(k) clearance on 2022-11-16 under approval number K222628. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Life Spine ALIF Buttress Plate System?

Life Spine ALIF Buttress Plate System is a medical device that received FDA 510(k) clearance on 2022-11-16. It is manufactured by Life Spine, Inc.. The 510(k) number is K222628.

When was Life Spine ALIF Buttress Plate System approved by the FDA?

Life Spine ALIF Buttress Plate System received FDA 510(k) clearance on 2022-11-16, under approval number K222628.

What company makes Life Spine ALIF Buttress Plate System?

Life Spine ALIF Buttress Plate System is manufactured by Life Spine, Inc..

What is the FDA product code for Life Spine ALIF Buttress Plate System?

The FDA product code for Life Spine ALIF Buttress Plate System is KWQ.

Related Clinical Trials

Other Devices by Life Spine, Inc.

View all 64 devices →

Related Devices (Code: KWQ)

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.