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

FDA 510(k)

CTS MIDCAB CORONARY SHUNT

K-Number: K963503 · 1997-04-03

Decision Date1997-04-03
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CTS MIDCAB CORONARY SHUNT is the device name listed in this FDA 510(k) record. The listed applicant is Cardiothoracic Systems, Inc.. It received FDA 510(k) clearance on 1997-04-03 under 510(k) number K963503. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CTS MIDCAB CORONARY SHUNT?

CTS MIDCAB CORONARY SHUNT is a medical device that received FDA 510(k) clearance on 1997-04-03. The listed applicant is Cardiothoracic Systems, Inc.. The 510(k) number is K963503.

When did CTS MIDCAB CORONARY SHUNT receive FDA 510(k) clearance?

CTS MIDCAB CORONARY SHUNT received FDA 510(k) clearance on 1997-04-03, under 510(k) number K963503.

Who is the listed applicant for CTS MIDCAB CORONARY SHUNT?

The FDA 510(k) record lists Cardiothoracic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CTS MIDCAB CORONARY SHUNT?

The FDA product code for CTS MIDCAB CORONARY SHUNT is DXC.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Cardiothoracic Systems, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 8 devices →

Related Devices (Code: DXC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

↑