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FDA 510(k)

AXYA SUTURE WELDING SYSTEM AND KIT

K-Number: K070253 · 2007-07-11

Decision Date2007-07-11
Product CodeGAT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AXYA SUTURE WELDING SYSTEM AND KIT is the device name listed in this FDA 510(k) record. The listed applicant is Axya Medical, Inc.. It received FDA 510(k) clearance on 2007-07-11 under 510(k) number K070253. The device is classified under product code GAT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 19 devices →

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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