AXYA SUTURE WELDING SYSTEM AND KIT
K-Number: K070253 · 2007-07-11
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Device Summary
Frequently Asked Questions
What is the AXYA SUTURE WELDING SYSTEM AND KIT?
AXYA SUTURE WELDING SYSTEM AND KIT is a medical device that received FDA 510(k) clearance on 2007-07-11. The listed applicant is Axya Medical, Inc.. The 510(k) number is K070253.
When did AXYA SUTURE WELDING SYSTEM AND KIT receive FDA 510(k) clearance?
AXYA SUTURE WELDING SYSTEM AND KIT received FDA 510(k) clearance on 2007-07-11, under 510(k) number K070253.
Who is the listed applicant for AXYA SUTURE WELDING SYSTEM AND KIT?
The FDA 510(k) record lists Axya Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AXYA SUTURE WELDING SYSTEM AND KIT?
The FDA product code for AXYA SUTURE WELDING SYSTEM AND KIT is GAT.
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 Axya Medical, 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: GAT)
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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