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FDA 510(k)

AXYAFLEX POLYESTER SUTURE

K-Number: K060165 · 2006-09-01

Decision Date2006-09-01
Product CodeGAT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AXYAFLEX POLYESTER SUTURE 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 2006-09-01 under 510(k) number K060165. 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 AXYAFLEX POLYESTER SUTURE?

AXYAFLEX POLYESTER SUTURE is a medical device that received FDA 510(k) clearance on 2006-09-01. The listed applicant is Axya Medical, Inc.. The 510(k) number is K060165.

When did AXYAFLEX POLYESTER SUTURE receive FDA 510(k) clearance?

AXYAFLEX POLYESTER SUTURE received FDA 510(k) clearance on 2006-09-01, under 510(k) number K060165.

Who is the listed applicant for AXYAFLEX POLYESTER SUTURE?

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 AXYAFLEX POLYESTER SUTURE?

The FDA product code for AXYAFLEX POLYESTER SUTURE 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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