Trifix Pedicle Spinal Screw Assembly

FDA 510(k) K990657 · Corin USA

Substantially Equivalent

510(k) numberK990657

Submission

Device name
Trifix Pedicle Spinal Screw Assembly
Applicant
Corin USA
Tampa, FL, US
Received
March 1, 1999
Decision date
March 26, 1999
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) statement 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

Other 510(k)s with product code MNH

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K162066Reliance Spinal Screw SystemMNH · Traditional Reliance Medical Systems, LLC12/02/2016SE
K162801CastleLoc Spinal Fixation SystemMNH · Special L&K BIOMED Co., Ltd.11/03/2016SE
K162143FixxSure® X-LinkMNH · Traditional Innovasis, Inc.09/23/2016SE
K161151Spinal fixation systemMNH · Traditional Canwell Medical Co., Ltd.09/21/2016SE
K162189ANAX™ 5.5 Spinal SystemMNH · Special U&I Corporation08/30/2016SE
K151362HC Spinal SystemMNH · Traditional Hung Chun Bio-S Co., Ltd.05/05/2016SE
K153404Zavation Spinal SystemMNH · Traditional Zavation, LLC04/21/2016SE
K160020Captiva Spine and CapLOX II/TowerLOX Pedicle Screw SystemMNH · Special Captiva Spine03/02/2016SE
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 Trifix Pedicle Spinal Screw Assembly cleared by the FDA?

Trifix Pedicle Spinal Screw Assembly (K990657) received a 510(k) decision of Substantially Equivalent on March 26, 1999, 25 days after the submission was received.

What is the product code of K990657?

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