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FDA 510(k)

CONMED LINVATEC ANODIZED ALUMINUM STERILIZATION TRAYS

K-Number: K090560 · 2009-06-29

Decision Date2009-06-29
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CONMED LINVATEC ANODIZED ALUMINUM STERILIZATION TRAYS is the device name listed in this FDA 510(k) record. The listed applicant is Conmed Linvatec. It received FDA 510(k) clearance on 2009-06-29 under 510(k) number K090560. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONMED LINVATEC ANODIZED ALUMINUM STERILIZATION TRAYS?

CONMED LINVATEC ANODIZED ALUMINUM STERILIZATION TRAYS is a medical device that received FDA 510(k) clearance on 2009-06-29. The listed applicant is Conmed Linvatec. The 510(k) number is K090560.

When did CONMED LINVATEC ANODIZED ALUMINUM STERILIZATION TRAYS receive FDA 510(k) clearance?

CONMED LINVATEC ANODIZED ALUMINUM STERILIZATION TRAYS received FDA 510(k) clearance on 2009-06-29, under 510(k) number K090560.

Who is the listed applicant for CONMED LINVATEC ANODIZED ALUMINUM STERILIZATION TRAYS?

The FDA 510(k) record lists Conmed Linvatec as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONMED LINVATEC ANODIZED ALUMINUM STERILIZATION TRAYS?

The FDA product code for CONMED LINVATEC ANODIZED ALUMINUM STERILIZATION TRAYS is KCT.

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 Conmed Linvatec 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: KCT)

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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