Aesculap Abc Cervical Plating System

FDA 510(k) K974706 · Aesculap, Inc.

Substantially Equivalent for Some Indications

510(k) numberK974706

Submission

Device name
Aesculap Abc Cervical Plating System
Applicant
Aesculap, Inc.
South San Francisco, CA, US
Received
December 16, 1997
Decision date
March 13, 1998
Decision
Substantially Equivalent for Some Indications (SN)
Type
Traditional 510(k)

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

Other 510(k)s with product code KWQ

510(k)DeviceApplicantDecision
K261309Palisades™ Buttress Plate SystemKWQ · Traditional Bethesda Medical Devices, LLC07/16/2026SE
K252776ARIES Anterior Cervical Plate SystemsKWQ · Traditional ZheJiang Decans Medical Devices Co., Ltd.05/14/2026SE
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

More from Carlsmed, Inc.

510(k)DeviceDecision
K242762Aesculap Aicon® Series Container SystemKCT · Traditional 05/13/2025SE
K242003XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter SetJXG · Traditional 12/16/2024SE
K223596SQ.line KERRISONHAE · Traditional 06/29/2023SE
K214041Aesculap AICON ContainerKCT · Traditional 12/30/2022SE
K211572Aesculap Slim Clip ApplierHCI · Traditional 12/13/2021SE
K203739ELAN 4 Electro Motor SystemHBE · Traditional 08/24/2021SE
K202391Dir 800IZI · Traditional 01/21/2021SE
K203461Aesculap Caiman 12 Seal and Cut Technology SystemGEI · Special 12/18/2020SE
K202938Aesculap Caiman 5 Seal and Cut Technology SystemGEI · Special 10/30/2020SE
K202124Aesculap PAS-Port Proximal Anastomosis SystemFZP · Special 09/02/2020SE

Questions and answers

When was Aesculap Abc Cervical Plating System cleared by the FDA?

Aesculap Abc Cervical Plating System (K974706) received a 510(k) decision of Substantially Equivalent for Some Indications on March 13, 1998, 87 days after the submission was received.

What is the product code of K974706?

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