PERIPHERAL AVE STENT SYSTEM
K-Number: K983008 · 1998-11-25
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Device Summary
Frequently Asked Questions
What is the PERIPHERAL AVE STENT SYSTEM?
PERIPHERAL AVE STENT SYSTEM is a medical device that received FDA 510(k) clearance on 1998-11-25. The listed applicant is Peripheral Ave. The 510(k) number is K983008.
When did PERIPHERAL AVE STENT SYSTEM receive FDA 510(k) clearance?
PERIPHERAL AVE STENT SYSTEM received FDA 510(k) clearance on 1998-11-25, under 510(k) number K983008.
Who is the listed applicant for PERIPHERAL AVE STENT SYSTEM?
The FDA 510(k) record lists Peripheral Ave as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PERIPHERAL AVE STENT SYSTEM?
The FDA product code for PERIPHERAL AVE STENT 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 Peripheral Ave 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.
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