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FDA 510(k)

2 Hole Lateral Plating System

K-Number: K172131 · 2017-08-28

Decision Date2017-08-28
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

2 Hole Lateral Plating System is the device name listed in this FDA 510(k) record. The listed applicant is Life Spine, Inc.. It received FDA 510(k) clearance on 2017-08-28 under 510(k) number K172131. 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 2 Hole Lateral Plating System?

2 Hole Lateral Plating System is a medical device that received FDA 510(k) clearance on 2017-08-28. The listed applicant is Life Spine, Inc.. The 510(k) number is K172131.

When did 2 Hole Lateral Plating System receive FDA 510(k) clearance?

2 Hole Lateral Plating System received FDA 510(k) clearance on 2017-08-28, under 510(k) number K172131.

Who is the listed applicant for 2 Hole Lateral Plating System?

The FDA 510(k) record lists Life Spine, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 2 Hole Lateral Plating System?

The FDA product code for 2 Hole Lateral Plating System is KWQ.

Other records listing Life Spine, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: KWQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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