Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PMMA BLOCK

K-Number: K223706 · 2023-05-12

Decision Date2023-05-12
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PMMA BLOCK is a medical device manufactured by Huliang(Shanghai) Bio-Tech Co., Ltd.. It received FDA 510(k) clearance on 2023-05-12 under approval number K223706. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PMMA BLOCK?

PMMA BLOCK is a medical device that received FDA 510(k) clearance on 2023-05-12. It is manufactured by Huliang(Shanghai) Bio-Tech Co., Ltd.. The 510(k) number is K223706.

When was PMMA BLOCK approved by the FDA?

PMMA BLOCK received FDA 510(k) clearance on 2023-05-12, under approval number K223706.

What company makes PMMA BLOCK?

PMMA BLOCK is manufactured by Huliang(Shanghai) Bio-Tech Co., Ltd..

What is the FDA product code for PMMA BLOCK?

The FDA product code for PMMA BLOCK is EBG.

Related Devices (Code: EBG)

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.