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FDA 510(k), K200805, Neocis Guidance System (NGS) with Patient Splints
FDA 510(k), K200805, Neocis Guidance System (NGS) with Patient Splints
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$149.00 USD
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510(K) Number: K200805
Device Name: Neocis Guidance System (NGS) with Patient Splints
Manufacturer: Neocis Inc.
Device Classification Name: Dental Stereotaxic Instrument
Regulation Number: 872.4120
Classification Product Code: PLV
Date Received: 03/27/2020
Decision Date: 07/28/2020
Regulation Medical Specialty: Dental
Device Name: Neocis Guidance System (NGS) with Patient Splints
Manufacturer: Neocis Inc.
Device Classification Name: Dental Stereotaxic Instrument
Regulation Number: 872.4120
Classification Product Code: PLV
Date Received: 03/27/2020
Decision Date: 07/28/2020
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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