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FDA 510(k), K202264, Neocis Guidance System (NGS) with Yomi Plan v2.0
FDA 510(k), K202264, Neocis Guidance System (NGS) with Yomi Plan v2.0
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510(K) Number: K202264
Device Name: Neocis Guidance System (NGS) with Yomi Plan v2.0
Manufacturer: Neocis Inc.
Device Classification Name: Dental Stereotaxic Instrument
Regulation Number: 872.4120
Classification Product Code: PLV
Date Received: 08/11/2020
Decision Date: 12/04/2020
Regulation Medical Specialty: Dental
Device Name: Neocis Guidance System (NGS) with Yomi Plan v2.0
Manufacturer: Neocis Inc.
Device Classification Name: Dental Stereotaxic Instrument
Regulation Number: 872.4120
Classification Product Code: PLV
Date Received: 08/11/2020
Decision Date: 12/04/2020
Regulation Medical Specialty: Dental
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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