FDA 510(k), K203401, Neocis Guidance System (NGS) with Patient Splints (EPS)

FDA 510(k), K203401, Neocis Guidance System (NGS) with Patient Splints (EPS)

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510(K) Number: K203401
Device Name: Neocis Guidance System (NGS) with Patient Splints (EPS)
Manufacturer: Neocis Inc.
Device Classification Name: Dental Stereotaxic Instrument
Regulation Number: 872.4120
Classification Product Code: PLV
Date Received: 11/19/2020
Decision Date: 12/15/2020
Regulation Medical Specialty: Dental

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