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FDA 510(k)

Novapak Nasal Sinus Packing and Stent

K-Number: K202623 · 2020-12-08

Decision Date2020-12-08
Product CodeLYA
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

Novapak Nasal Sinus Packing and Stent is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Xomed. It received FDA 510(k) clearance on 2020-12-08 under 510(k) number K202623. The device is classified under product code LYA. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Novapak Nasal Sinus Packing and Stent?

Novapak Nasal Sinus Packing and Stent is a medical device that received FDA 510(k) clearance on 2020-12-08. The listed applicant is Medtronic Xomed. The 510(k) number is K202623.

When did Novapak Nasal Sinus Packing and Stent receive FDA 510(k) clearance?

Novapak Nasal Sinus Packing and Stent received FDA 510(k) clearance on 2020-12-08, under 510(k) number K202623.

Who is the listed applicant for Novapak Nasal Sinus Packing and Stent?

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

What is the FDA product code for Novapak Nasal Sinus Packing and Stent?

The FDA product code for Novapak Nasal Sinus Packing and Stent is LYA.

Related Clinical Trials

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.

Other records listing Medtronic Xomed 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.

View all 8 devices →

Related Devices (Code: LYA)

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.

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.