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FDA 510(k)

SINGLE PLANAR MULTI AXIAL (SPMA) PEDICLE SCREW SYSTEM

K-Number: K070295 · 2007-05-21

ApplicantTrinity Orthopedics, LLC
Decision Date2007-05-21
Product CodeMNI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SINGLE PLANAR MULTI AXIAL (SPMA) PEDICLE SCREW SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Trinity Orthopedics, LLC. It received FDA 510(k) clearance on 2007-05-21 under 510(k) number K070295. The device is classified under product code MNI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SINGLE PLANAR MULTI AXIAL (SPMA) PEDICLE SCREW SYSTEM?

SINGLE PLANAR MULTI AXIAL (SPMA) PEDICLE SCREW SYSTEM is a medical device that received FDA 510(k) clearance on 2007-05-21. The listed applicant is Trinity Orthopedics, LLC. The 510(k) number is K070295.

When did SINGLE PLANAR MULTI AXIAL (SPMA) PEDICLE SCREW SYSTEM receive FDA 510(k) clearance?

SINGLE PLANAR MULTI AXIAL (SPMA) PEDICLE SCREW SYSTEM received FDA 510(k) clearance on 2007-05-21, under 510(k) number K070295.

Who is the listed applicant for SINGLE PLANAR MULTI AXIAL (SPMA) PEDICLE SCREW SYSTEM?

The FDA 510(k) record lists Trinity Orthopedics, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SINGLE PLANAR MULTI AXIAL (SPMA) PEDICLE SCREW SYSTEM?

The FDA product code for SINGLE PLANAR MULTI AXIAL (SPMA) PEDICLE SCREW SYSTEM is MNI.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Trinity Orthopedics, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K081790MODIFICATION TO SINGLE PLANAR MULTI AXIS (SPMA) PEDICLE SCREW SYSTEM

Related Devices (Code: MNI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K171497Mikron Spinal Fixation SystemMikron Makina Sanayi Ticaret Co. , Ltd.K160731LumFix Spinal Fixation SytemCG Bio Co., Ltd.K151458Double Medical Universal Spine SystemDouble Medical Technology, Inc.K153273MySpine Pedicle Screw Placement Guides - LPMedacta International S.A.K160124LUMIS Cannulated Pedicle Screw Fixation System, U.L.I.S. Pedicle Screw Fixation SystemSpinevision S.A.K160320PremierShandong Weigao Orthopaedic Device Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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