ARCHIMEDES Biodegradable Stent (Medium)
K-Number: K260835 · 2026-07-27
Device Summary
Frequently Asked Questions
What is the ARCHIMEDES Biodegradable Stent (Medium)?
ARCHIMEDES Biodegradable Stent (Medium) is a medical device that received FDA 510(k) clearance on 2026-07-27. The listed applicant is Q3 Medical USA, LLC (C/O Q3 Medical Devices Ltd.). The 510(k) number is K260835.
When did ARCHIMEDES Biodegradable Stent (Medium) receive FDA 510(k) clearance?
ARCHIMEDES Biodegradable Stent (Medium) received FDA 510(k) clearance on 2026-07-27, under 510(k) number K260835.
Who is the listed applicant for ARCHIMEDES Biodegradable Stent (Medium)?
The FDA 510(k) record lists Q3 Medical USA, LLC (C/O Q3 Medical Devices Ltd.) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARCHIMEDES Biodegradable Stent (Medium)?
The FDA product code for ARCHIMEDES Biodegradable Stent (Medium) 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 Q3 Medical USA, LLC (C/O Q3 Medical Devices Ltd.) 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.