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FDA 510(k)

Neocis Guidance System (NGS) with Fiducial Array Splint (FAS)

K-Number: K200348 · 2020-05-08

ApplicantNeocis, Inc.
Decision Date2020-05-08
Product CodePLV
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Neocis Guidance System (NGS) with Fiducial Array Splint (FAS) is a medical device manufactured by Neocis, Inc.. It received FDA 510(k) clearance on 2020-05-08 under approval number K200348. 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 Fiducial Array Splint (FAS)?

Neocis Guidance System (NGS) with Fiducial Array Splint (FAS) is a medical device that received FDA 510(k) clearance on 2020-05-08. It is manufactured by Neocis, Inc.. The 510(k) number is K200348.

When was Neocis Guidance System (NGS) with Fiducial Array Splint (FAS) approved by the FDA?

Neocis Guidance System (NGS) with Fiducial Array Splint (FAS) received FDA 510(k) clearance on 2020-05-08, under approval number K200348.

What company makes Neocis Guidance System (NGS) with Fiducial Array Splint (FAS)?

Neocis Guidance System (NGS) with Fiducial Array Splint (FAS) is manufactured by Neocis, Inc..

What is the FDA product code for Neocis Guidance System (NGS) with Fiducial Array Splint (FAS)?

The FDA product code for Neocis Guidance System (NGS) with Fiducial Array Splint (FAS) 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.