Osteonics Spinal System

FDA 510(k) K020293 · Howmedica Osteonics Corp.

Substantially Equivalent

510(k) numberK020293

Submission

Device name
Osteonics Spinal System
Applicant
Howmedica Osteonics Corp.
Allendale, NJ, US
Received
January 28, 2002
Decision date
February 14, 2002
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MNH – Orthosis, Spondylolisthesis Spinal Fixation
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3070
Specialty
Orthopedic
Implant
Yes

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K143013Spinal Inner Fixation SystemMNH · Traditional Changzhou Dingjian Medical Appliance Co., Ltd.12/11/2015SE
K151695Romeo posterior osteosynthesis systemMNH · Traditional Spineart09/10/2015SE

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Questions and answers

When was Osteonics Spinal System cleared by the FDA?

Osteonics Spinal System (K020293) received a 510(k) decision of Substantially Equivalent on February 14, 2002, 17 days after the submission was received.

What is the product code of K020293?

The FDA product code is MNH – Orthosis, Spondylolisthesis Spinal Fixation, a Class II (moderate risk) device regulated under 21 CFR 888.3070.