Osteonics Spinal System 5.5MM & 10.0MM Bone Screws

FDA 510(k) K983152 · Osteonics Corp.

Substantially Equivalent

510(k) numberK983152

Submission

Device name
Osteonics Spinal System 5.5MM & 10.0MM Bone Screws
Applicant
Osteonics Corp.
Allendale, NJ, US
Received
September 9, 1998
Decision date
September 25, 1998
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
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Questions and answers

When was Osteonics Spinal System 5.5MM & 10.0MM Bone Screws cleared by the FDA?

Osteonics Spinal System 5.5MM & 10.0MM Bone Screws (K983152) received a 510(k) decision of Substantially Equivalent on September 25, 1998, 16 days after the submission was received.

What is the product code of K983152?

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