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FDA 510(k)

CODA™ Anterior Cervical Plate System

K-Number: K222493 · 2022-11-18

ApplicantPioneer Surgical Technology, Inc.
Decision Date2022-11-18
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CODA™ Anterior Cervical Plate System is the device name listed in this FDA 510(k) record. The listed applicant is Pioneer Surgical Technology, Inc.. It received FDA 510(k) clearance on 2022-11-18 under 510(k) number K222493. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CODA™ Anterior Cervical Plate System?

CODA™ Anterior Cervical Plate System is a medical device that received FDA 510(k) clearance on 2022-11-18. The listed applicant is Pioneer Surgical Technology, Inc.. The 510(k) number is K222493.

When did CODA™ Anterior Cervical Plate System receive FDA 510(k) clearance?

CODA™ Anterior Cervical Plate System received FDA 510(k) clearance on 2022-11-18, under 510(k) number K222493.

Who is the listed applicant for CODA™ Anterior Cervical Plate System?

The FDA 510(k) record lists Pioneer Surgical Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CODA™ Anterior Cervical Plate System?

The FDA product code for CODA™ Anterior Cervical Plate System is KWQ.

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.

NCT05762055Prospective Comparative Analysis of ACDF vs Fusion Interbody Cages With nanoLOCK Osseointegrative TechnologyENROLLING_BY_INVITATION

Other records listing Pioneer Surgical Technology, Inc. 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.

K261271Cable-Ready® Cable Grip SystemK251436Resolve Anterior Cervical Plate SystemK211408CervAlign® Anterior Cervical Plate SystemK192396Streamline MIS Spinal Fixation System

Related Devices (Code: KWQ)

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.

K261309Palisades™ Buttress Plate SystemBethesda Medical Devices, LLCK252776ARIES Anterior Cervical Plate SystemsZheJiang Decans Medical Devices Co., Ltd.K261112CastleLoc-P Anterior Cervical Plate SystemL&K BIOMED Co., Ltd.K260570corra™ cervical plating systemCarlsmed, Inc.K260697VyPlate™ Anterior Cervical Plate SystemVy Spine, LLCK260015ANTERIS Thoracolumbar Plate SystemSpineCraft

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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