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FDA 510(k)

Parcus Titanium Interference Screws

K-Number: K202662 · 2021-02-22

ApplicantParcus Medical, LLC
Decision Date2021-02-22
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Parcus Titanium Interference Screws is a medical device manufactured by Parcus Medical, LLC. It received FDA 510(k) clearance on 2021-02-22 under approval number K202662. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Parcus Titanium Interference Screws?

Parcus Titanium Interference Screws is a medical device that received FDA 510(k) clearance on 2021-02-22. It is manufactured by Parcus Medical, LLC. The 510(k) number is K202662.

When was Parcus Titanium Interference Screws approved by the FDA?

Parcus Titanium Interference Screws received FDA 510(k) clearance on 2021-02-22, under approval number K202662.

What company makes Parcus Titanium Interference Screws?

Parcus Titanium Interference Screws is manufactured by Parcus Medical, LLC.

What is the FDA product code for Parcus Titanium Interference Screws?

The FDA product code for Parcus Titanium Interference Screws is MBI.

Related Clinical Trials

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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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