Tricos T Resorbable Bone Substitute

by Baxter Healthcare Corporation 510(k)

Active United States

510(k) K073571

Regulatory status

as of 27 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Abbreviated	NumberK073571	Date8 Apr 2008Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not known
Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 24 Oct 2026.

Specification

510(k)

510(k) Number: K073571
FDA Product Code: LYC

Device Class: Class II
Regulation: 21 CFR Part 872.3930
Advisory Committee: Dental
FDA Decision: SESE Substantially Equivalent

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