510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K073571Substantially Equivalent

Tricos T Resorbable Bone Substitute

Baxter Healthcare Corporation, Mcgaw Park IL / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K073571 is the FDA 510(k) clearance record for TRICOS T RESORBABLE BONE SUBSTITUTE, a class II device, cleared for Baxter Healthcare Corporation on under FDA product code LYC (Bone Grafting Material, Synthetic). FDA's definition for product code LYC reads: "A synthetic bone grafting material is synthetically-derived device, such as hydroxylapatite, intended to fill, augment, or reconstruct periodontal and or bony defects of the upper or lower jaw". FDA records list 570 510(k) clearances for Baxter Healthcare Corporation, from to . As of , FDA records show no recalls naming K073571.

Clearance record

Decision date
Received
(110 days to decision)
Product code
LYC Bone Grafting Material, Synthetic
Regulation
21 CFR 872.3930
Device class
Class II
Review panel
Dental
Applicant
Baxter Healthcare Corporation 1620 Waukegan Rd., Mpgr-Al, Mcgaw Park IL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LYC

Trailing 12 months
3 clearances under product code LYC in the twelve months to November 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code LYC, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20261
April 20260
May 20261
June 20260
July 20261
August 20260
September 20260
October 20260
November 20260