FDA 510(k), K202100, Neocis Guidance System (NGS) with Clamped Chairside Patient Splint (C-CPS)
FDA 510(k), K202100, Neocis Guidance System (NGS) with Clamped Chairside Patient Splint (C-CPS)
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510(K) Number: K202100
Device Name: Neocis Guidance System (NGS) with Clamped Chairside Patient Splint (C-CPS)
Manufacturer: Neocis Inc.
Device Classification Name: Dental Stereotaxic Instrument
Regulation Number: 872.4120
Classification Product Code: PLV
Date Received: 07/29/2020
Decision Date: 10/19/2020
Regulation Medical Specialty: Dental
Device Name: Neocis Guidance System (NGS) with Clamped Chairside Patient Splint (C-CPS)
Manufacturer: Neocis Inc.
Device Classification Name: Dental Stereotaxic Instrument
Regulation Number: 872.4120
Classification Product Code: PLV
Date Received: 07/29/2020
Decision Date: 10/19/2020
Regulation Medical Specialty: Dental
- 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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