PRIMUS STENT AND DELIVERY SYSTEM
K-Number: K043243 · 2004-12-09
Advertisement
Device Summary
Frequently Asked Questions
What is the PRIMUS STENT AND DELIVERY SYSTEM?
PRIMUS STENT AND DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 2004-12-09. The listed applicant is Ev3, Inc.. The 510(k) number is K043243.
When did PRIMUS STENT AND DELIVERY SYSTEM receive FDA 510(k) clearance?
PRIMUS STENT AND DELIVERY SYSTEM received FDA 510(k) clearance on 2004-12-09, under 510(k) number K043243.
Who is the listed applicant for PRIMUS STENT AND DELIVERY SYSTEM?
The FDA 510(k) record lists Ev3, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PRIMUS STENT AND DELIVERY SYSTEM?
The FDA product code for PRIMUS STENT AND DELIVERY SYSTEM is FGE.
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 Ev3, 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.
Related Devices (Code: FGE)
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.
Advertisement