Neocis Guidance System (NGS) with Clamped Chairside Patient Splint (C-CPS)
K-Number: K202100 · 2020-10-19
Device Summary
Frequently Asked Questions
What is the Neocis Guidance System (NGS) with Clamped Chairside Patient Splint (C-CPS)?
Neocis Guidance System (NGS) with Clamped Chairside Patient Splint (C-CPS) is a medical device that received FDA 510(k) clearance on 2020-10-19. It is manufactured by Neocis, Inc.. The 510(k) number is K202100.
When was Neocis Guidance System (NGS) with Clamped Chairside Patient Splint (C-CPS) approved by the FDA?
Neocis Guidance System (NGS) with Clamped Chairside Patient Splint (C-CPS) received FDA 510(k) clearance on 2020-10-19, under approval number K202100.
What company makes Neocis Guidance System (NGS) with Clamped Chairside Patient Splint (C-CPS)?
Neocis Guidance System (NGS) with Clamped Chairside Patient Splint (C-CPS) is manufactured by Neocis, Inc..
What is the FDA product code for Neocis Guidance System (NGS) with Clamped Chairside Patient Splint (C-CPS)?
The FDA product code for Neocis Guidance System (NGS) with Clamped Chairside Patient Splint (C-CPS) is PLV.
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Related PubMed Literature
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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.