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FDA PMA

SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS

PMA Number: P930031 · 2024-06-27

ApplicantBoston Scientific Corp
Decision Date2024-06-27
PMA NumberP930031
Product CodeMIR
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeCV

Device Summary

SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corp. It received FDA 510(k) clearance on 2024-06-27. The device is classified under product code MIR. It was reviewed by the CV advisory panel.

Frequently Asked Questions

What is the SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS?

SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS is a medical device that received FDA 510(k) clearance on 2024-06-27. The listed applicant is Boston Scientific Corp.

When did SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS receive FDA 510(k) clearance?

The clearance date for SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS can be found in the official FDA records.

Who is the listed applicant for SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS?

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

What is the FDA product code for SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS?

The FDA product code for SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS is MIR.

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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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