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FDA 510(k)

STERI-OSS Implant System

K-Number: K232268 · 2024-03-25

Decision Date2024-03-25
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

STERI-OSS Implant System is a medical device manufactured by Zeros Co., Ltd.. It received FDA 510(k) clearance on 2024-03-25 under approval number K232268. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERI-OSS Implant System?

STERI-OSS Implant System is a medical device that received FDA 510(k) clearance on 2024-03-25. It is manufactured by Zeros Co., Ltd.. The 510(k) number is K232268.

When was STERI-OSS Implant System approved by the FDA?

STERI-OSS Implant System received FDA 510(k) clearance on 2024-03-25, under approval number K232268.

What company makes STERI-OSS Implant System?

STERI-OSS Implant System is manufactured by Zeros Co., Ltd..

What is the FDA product code for STERI-OSS Implant System?

The FDA product code for STERI-OSS Implant System is DZE.

Related Clinical Trials

Related PubMed Literature

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Official Source

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