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FDA 510(k)

Reform® POCT System

K-Number: K172495 · 2018-04-11

ApplicantPrecision Spine, Inc.
Decision Date2018-04-11
Product CodeNKG
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Reform® POCT System is the device name listed in this FDA 510(k) record. The listed applicant is Precision Spine, Inc.. It received FDA 510(k) clearance on 2018-04-11 under 510(k) number K172495. The device is classified under product code NKG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Reform® POCT System?

Reform® POCT System is a medical device that received FDA 510(k) clearance on 2018-04-11. The listed applicant is Precision Spine, Inc.. The 510(k) number is K172495.

When did Reform® POCT System receive FDA 510(k) clearance?

Reform® POCT System received FDA 510(k) clearance on 2018-04-11, under 510(k) number K172495.

Who is the listed applicant for Reform® POCT System?

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

What is the FDA product code for Reform® POCT System?

The FDA product code for Reform® POCT System is NKG.

Other records listing Precision Spine, Inc. as applicant

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Related Devices (Code: NKG)

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.

K253195TAURUS Posterior Occipital-Cervico-Thoracic Spinal SystemsZheJiang Decans Medical Devices Co., Ltd.K254045CarboClear® Posterior Cervical Screw System; CarboClear® Hybrid Posterior Cervical Screw SystemCarboFix Orthopedics , Ltd.K254165Infinity™ OCT SystemMedtronic Sofamor Danek USA, Inc.K252327CMORE® CT System; CMORE® CT System Navigated InstrumentsIcotec AGK253129Infinity™ OCT SystemMedtronic Sofamor Danek USA, Inc.K251725ANAX™ OCT Spinal SystemCg Medtech 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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