Osteonics Anterior Cervical Compression Plating System

FDA 510(k) K982798 · Osteonics Corp.

Substantially Equivalent

510(k) numberK982798

Submission

Device name
Osteonics Anterior Cervical Compression Plating System
Applicant
Osteonics Corp.
Allendale, NJ, US
Received
August 10, 1998
Decision date
March 25, 1999
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KWQ – Appliance, Fixation, Spinal Intervertebral Body
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3060
Specialty
Orthopedic
Implant
Yes

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K261112CastleLoc-P Anterior Cervical Plate SystemKWQ · Special L&K BIOMED Co., Ltd.05/06/2026SE
K260570corra™ cervical plating systemKWQ · Traditional Carlsmed, Inc.04/22/2026SE
K260697VyPlate™ Anterior Cervical Plate SystemKWQ · Special Vy Spine, LLC03/27/2026SE
K260015ANTERIS Thoracolumbar Plate SystemKWQ · Traditional SpineCraft03/04/2026SE
K251940PathLoc Lumbar Plate SystemKWQ · Traditional L&K BIOMED Co., Ltd.03/03/2026SE
K254182AsterKWQ · Traditional Osteonic Co., Ltd.02/26/2026SE
K253201Lumbar Spine Truss System - Plating Solution (LSTS-PS)KWQ · Special 4Web, Inc.02/12/2026SE
K252611aprevo® cervical plating systemKWQ · Traditional Carlsmed, Inc.12/22/2025SE

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K990158Osteonics Combination Screw Ring/BlockerMNI · Special 02/01/1999SE
K984302Osteonics Spinal System Cylindrical Bone ScrewsMNH · Special 12/18/1998SE
K984353Osteo 9MM Ic Tibial NailHSB · Special 12/16/1998SE
K983502Osteonics Secur-Fit Ad Generation II Acetabular Component SystemLPH · Traditional 12/16/1998SE
K983382Osteonics Ha Generation II Acetabular Component SystemMEH · Traditional 12/11/1998SE

Questions and answers

When was Osteonics Anterior Cervical Compression Plating System cleared by the FDA?

Osteonics Anterior Cervical Compression Plating System (K982798) received a 510(k) decision of Substantially Equivalent on March 25, 1999, 227 days after the submission was received.

What is the product code of K982798?

The FDA product code is KWQ – Appliance, Fixation, Spinal Intervertebral Body, a Class II (moderate risk) device regulated under 21 CFR 888.3060.