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FDA 510(k)

Neocis Guidance System (NGS) with Clamped Chairside Patient Splint (C-CPS)

K-Number: K202100 · 2020-10-19

ApplicantNeocis, Inc.
Decision Date2020-10-19
Product CodePLV
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Neocis Guidance System (NGS) with Clamped Chairside Patient Splint (C-CPS) is a medical device manufactured by Neocis, Inc.. It received FDA 510(k) clearance on 2020-10-19 under approval number K202100. The device is classified under product code PLV. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

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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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.