FDA 510(k)

Barricaid Instrument Tray

K-Number: K201676 · 2020-07-16

Decision Date2020-07-16

Product CodeQHG

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

Barricaid Instrument Tray is the device name listed in this FDA 510(k) record. The listed applicant is Intrinsic Therapeutics, Inc.. It received FDA 510(k) clearance on 2020-07-16 under 510(k) number K201676. The device is classified under product code QHG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Barricaid Instrument Tray?

Barricaid Instrument Tray is a medical device that received FDA 510(k) clearance on 2020-07-16. The listed applicant is Intrinsic Therapeutics, Inc.. The 510(k) number is K201676.

When did Barricaid Instrument Tray receive FDA 510(k) clearance?

Barricaid Instrument Tray received FDA 510(k) clearance on 2020-07-16, under 510(k) number K201676.

Who is the listed applicant for Barricaid Instrument Tray?

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

What is the FDA product code for Barricaid Instrument Tray?

The FDA product code for Barricaid Instrument Tray is QHG.

Other records listing Intrinsic Therapeutics, Inc. as applicant

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.

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Official Source

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