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FDA 510(k)

Novapak Nasal Sinus Packing and Stent

K-Number: K202623 · 2020-12-08

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

Device Summary

Novapak Nasal Sinus Packing and Stent is a medical device manufactured by Medtronic Xomed. It received FDA 510(k) clearance on 2020-12-08 under approval 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. It is manufactured by Medtronic Xomed. The 510(k) number is K202623.

When was Novapak Nasal Sinus Packing and Stent approved by the FDA?

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

What company makes Novapak Nasal Sinus Packing and Stent?

Novapak Nasal Sinus Packing and Stent is manufactured by Medtronic Xomed.

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.

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Related Devices (Code: LYA)

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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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