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FDA 510(k)

TRICOS A RESORBABLE SUBSTITUTE

K-Number: K081721 · 2008-08-06

ApplicantBaxter Healthcare Corp
Decision Date2008-08-06
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TRICOS A RESORBABLE SUBSTITUTE is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 2008-08-06 under 510(k) number K081721. The device is classified under product code LYC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRICOS A RESORBABLE SUBSTITUTE?

TRICOS A RESORBABLE SUBSTITUTE is a medical device that received FDA 510(k) clearance on 2008-08-06. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K081721.

When did TRICOS A RESORBABLE SUBSTITUTE receive FDA 510(k) clearance?

TRICOS A RESORBABLE SUBSTITUTE received FDA 510(k) clearance on 2008-08-06, under 510(k) number K081721.

Who is the listed applicant for TRICOS A RESORBABLE SUBSTITUTE?

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

What is the FDA product code for TRICOS A RESORBABLE SUBSTITUTE?

The FDA product code for TRICOS A RESORBABLE SUBSTITUTE is LYC.

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Related Devices (Code: LYC)

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.

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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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