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FDA 510(k)

AMT T-FASTENER ANCHOR KIT

K-Number: K120587 · 2012-05-25

Decision Date2012-05-25
Product CodeKGC
Advisory CommitteeGU
DecisionUnknown

Device Summary

AMT T-FASTENER ANCHOR KIT is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Technology, Inc.. It received FDA 510(k) clearance on 2012-05-25 under 510(k) number K120587. The device is classified under product code KGC. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the AMT T-FASTENER ANCHOR KIT?

AMT T-FASTENER ANCHOR KIT is a medical device that received FDA 510(k) clearance on 2012-05-25. The listed applicant is Applied Medical Technology, Inc.. The 510(k) number is K120587.

When did AMT T-FASTENER ANCHOR KIT receive FDA 510(k) clearance?

AMT T-FASTENER ANCHOR KIT received FDA 510(k) clearance on 2012-05-25, under 510(k) number K120587.

Who is the listed applicant for AMT T-FASTENER ANCHOR KIT?

The FDA 510(k) record lists Applied Medical Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMT T-FASTENER ANCHOR KIT?

The FDA product code for AMT T-FASTENER ANCHOR KIT is KGC.

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 Applied Medical Technology, 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 21 devices →

Related Devices (Code: KGC)

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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