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Tricos T

by Baxter Healthcare Corp

510(k) K051722

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK051722 Date18 Nov 2005ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
MQV
Device class
Class II
Regulation
21 CFR Part 888.3045
Advisory committee
Orthopedic
FDA decision
SESE Substantially Equivalent

Overview

AI-generated summary, 23 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

Tricos T is a resorbable bone substitute intended for use as a bone void filler. It is designed to fill bony voids or gaps of the skeletal system that are not intrinsic to the stability of the bony structure.

This device is supplied by Baxter Healthcare Corp and has received FDA 510(k) clearance. It is classified under the orthopedic advisory committee and is regulated as a bone void filler.

Other devices from Baxter Healthcare Corp

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Questions

AI-generated answers, 23 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

  • What is the intended use of Tricos T?

    Tricos T is indicated for use as a resorbable bone void filler. It is specifically designed to fill gaps or voids in the skeletal system that do not contribute to the overall stability of the bony structure.

  • Who is the manufacturer of this bone void filler?

    Tricos T is manufactured by Baxter Healthcare Corp, located in Westlake Village, California.

  • What is the regulatory status of Tricos T?

    Tricos T has received FDA 510(k) clearance. It is classified under the orthopedic advisory committee and is regulated as a bone void filler.