Swift Anterior Cervical Plate System

FDA 510(k) K040655 · Depuy Spine, Inc.

Substantially Equivalent

510(k) numberK040655

Submission

Device name
Swift Anterior Cervical Plate System
Applicant
Depuy Spine, Inc.
Raynham, MA, US
Received
March 12, 2004
Decision date
June 2, 2004
Decision
Substantially Equivalent (SESE)
Type
Special 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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Questions and answers

When was Swift Anterior Cervical Plate System cleared by the FDA?

Swift Anterior Cervical Plate System (K040655) received a 510(k) decision of Substantially Equivalent on June 2, 2004, 82 days after the submission was received.

What is the product code of K040655?

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