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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 the device name listed in this FDA 510(k) record. The listed applicant is Neocis, Inc.. It received FDA 510(k) clearance on 2020-10-19 under 510(k) 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. The listed applicant is Neocis, Inc.. The 510(k) number is K202100.

When did Neocis Guidance System (NGS) with Clamped Chairside Patient Splint (C-CPS) receive FDA 510(k) clearance?

Neocis Guidance System (NGS) with Clamped Chairside Patient Splint (C-CPS) received FDA 510(k) clearance on 2020-10-19, under 510(k) number K202100.

Who is the listed applicant for Neocis Guidance System (NGS) with Clamped Chairside Patient Splint (C-CPS)?

The FDA 510(k) record lists Neocis, Inc. as the applicant. This does not by itself establish the device manufacturer.

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.

Other records listing Neocis, Inc. as applicant

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Related Devices (Code: PLV)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K252376Yomi S Robotic SystemNeocis, Inc.K251835Yomi Robotic SystemNeocis, Inc.K233563NavidentClaronav, Inc.K231018Yomi Robotic SystemNeocis, Inc.K210947NavidentClaronav, Inc.K211466Yomi Robotic System with YomiPlan GoNeocis, Inc.

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.

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