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FDA 510(k)

2 Hole Lateral Plating System

K-Number: K172131 · 2017-08-28

ApplicantLife Spine, Inc.
Decision Date2017-08-28
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

2 Hole Lateral Plating System is a medical device manufactured by Life Spine, Inc.. It received FDA 510(k) clearance on 2017-08-28 under approval 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. It is manufactured by Life Spine, Inc.. The 510(k) number is K172131.

When was 2 Hole Lateral Plating System approved by the FDA?

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

What company makes 2 Hole Lateral Plating System?

2 Hole Lateral Plating System is manufactured by Life Spine, Inc..

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

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

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Other Devices by Life Spine, Inc.

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Related Devices (Code: KWQ)

K160982Sphynx™Eden Spine, LLC K162638CETRA Anterior Cervical Plate SystemOrthofix, Inc. K162194MEDICREA INTERNATIONAL Anterior Cervical Locking Plate SystemMedicrea International SA K162211AccuFit Lateral Plate SystemPrecision Spine, Inc. K162250FortiBridge Anterior Cervical Plate SystemNanovis Spine, LLC K162664Pyrenees Cervical Plate SystemK2m, Inc.

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.

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