510(k) Report

510(k) · Cleared

Cleared

Tricos T

K051722510(k) TraditionalCleared Nov 18, 2005144-day reviewClass II21 CFR 888.3045

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Baxter Healthcare Corp · MQV Filler, Bone Void, Calcium Compound

Cleared on Nov 18, 2005 as substantially equivalent to K032268 (Biomatlante, 2003) and 4 other predicates after a 144-day review. Its family tree reaches back 3 generations to 1999. 3 later devices descend from it.

Decided
Nov 18, 2005
Review
144 days
Class
Class II
Product code
MQV
Recalls
None
Predicates
5

Its longest line of descent runs back 3 generations to K990131 (1999). 10 ancestors in all. 3 later devices descend from it, 3 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2004: 3 other ancestors2001: 1 other ancestor2003: 2 other ancestors2000: 1 other ancestor2008: 3 descendants clearedK990131 · Pro Osteon Implant 500R Resorbable Bone Graft Substitute · Interpore Cross Intl. · 1999K020986 · Mastergraft Resorbable Ceramic · Medtronic Sofamor Danek, Inc. · 2002K032268 · MBCP · Biomatlante · 20031995200020052010201520202025
Other ancestors, by generationDescendants, by generation 1 generation back: 4 other ancestors2 generations back: 3 other ancestors 1 generation forward: 3 descendants K032268 · MBCP · Biomatlante · 2003K020986 · Mastergraft Resorbable Ceramic · Medtronic Sofamor Danek, Inc. · 2002K990131 · Pro Osteon Implant 500R Resorbable Bone Graft Substitute · Interpore Cross Intl. · 19990
  1. Root · 3 generations backK990131 Pro Osteon Implant 500R Resorbable Bone Graft SubstituteInterpore Cross Intl. · 1999
  2. 2 generations backK020986 Mastergraft Resorbable CeramicMedtronic Sofamor Danek, Inc. · 2002
  3. 1 generation backK032268 MBCPBiomatlante · 2003
  4. This deviceK051722 Tricos TBaxter Healthcare Corp · 2005
  5. Descendant · cites it directly · 2 of its ownK073571 Tricos T Resorbable Bone SubstituteBaxter Healthcare Corporation · 2008
  6. Descendant · cites it directly · 0 of its ownK081717 Tricos a Resorbable Bone SubstituteBaxter Healthcare Corp · 2008
  7. Descendant · cites it directly · 0 of its ownK081721 Tricos a Resorbable SubstituteBaxter Healthcare Corp · 2008

Most influential descendants

Showing 3 of 3 · See all
  • K073571Tricos T Resorbable Bone SubstituteBaxter Healthcare Corporation · 2008 · cites it directly2descendants
  • K081717Tricos a Resorbable Bone SubstituteBaxter Healthcare Corp · 2008 · cites it directly0descendants
  • K081721Tricos a Resorbable SubstituteBaxter Healthcare Corp · 2008 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K990131Pro Osteon Implant 500R Resorbable Bone Graft SubstituteInterpore Cross Intl.1999—
−2K020986Mastergraft Resorbable CeramicMedtronic Sofamor Danek, Inc.2002—
−1K032268MBCPBiomatlante2003—
0 (this device)K051722Tricos TBaxter Healthcare Corp2005—
+1K073571Tricos T Resorbable Bone SubstituteBaxter Healthcare Corporation2008—
+1K081717Tricos a Resorbable Bone SubstituteBaxter Healthcare Corp2008—
+1K081721Tricos a Resorbable SubstituteBaxter Healthcare Corp2008—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200010
200110
200320
200430

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200830
FIG. 1 — Lineage of K051722, 1999–2008Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in MQV? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new MQV device

  1. #1 K232315 Catalyst Bone Void Fillerscore 25.2 · 25 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (5)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K032268MBCP
Summary page 1
…le Calcium Salt Bone Void Filler (21 CFR Name: §888.3045) Predicate Device: MBCP BIOMATLANTE 5 10(k) K032268 Collagraft Strip Bone Graft Matrix NeuColl, Inc. 5 10(k) K0…
Biomatlante2003—
*K000122Collagraft Strip Bone Graft Matrix (for Use as a Bone Filler), Model 1X,3X,6X (1,3 or 6…
Summary page 1
…NTE 5 10(k) K032268 Collagraft Strip Bone Graft Matrix NeuColl, Inc. 5 10(k) K000 122 Allomatrix Putty Wright Medical Technology, Inc. 5 10(k) K0…
Neucoll, Inc.2001—
*K020895Allomatrix Model# 86
Summary page 1
…c. 5 10(k) K000 122 Allomatrix Putty Wright Medical Technology, Inc. 5 10(k) K020895 TCP Putty Stryker Biotech 5 10(k) K041421…
Wrightmedicaltechnologyinc2004—
*K041421Name Bone Void Filler
Summary page 1
…t Medical Technology, Inc. 5 10(k) K020895 TCP Putty Stryker Biotech 5 10(k) K041421 JAX-tcp Smith & Nephew, Inc. 510(k) K033552 Description of th…
Stryker Biotech20041
*K033552Jax-TCP
Summary page 1
…Stryker Biotech 5 10(k) K041421 JAX-tcp Smith & Nephew, Inc. 510(k) K033552 Description of the Device: TricOs T is a resorbable bone substitute that is replaced over time by newly formed bone. TricOs T co…
Smith & Nephew, Inc.2004—

Also cleared against K032268: 10 other devices →

What descends from it? (3)

3 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K073571Tricos T Resorbable Bone SubstituteBaxter Healthcare Corporation20082
K081717Tricos a Resorbable Bone SubstituteBaxter Healthcare Corp20080
K081721Tricos a Resorbable SubstituteBaxter Healthcare Corp20080

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 6 years and passes through 4 companies; a new generation was cleared every 1.9 years on median.
  • 2 of the 10 ancestors have a recall of any class.
  • Of its descendants, K073571 (Baxter Healthcare Corporation, 2008) has gone furthest, with 2 descendants of its own.
  • 10 other devices also cite its predicate K032268.

How does its category compare?

All MQV devices

MQV Filler, Bone Void, Calcium Compound: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · MQV

14in 2025

2007: 352008: 322009: 232010: 172011: 162012: 92013: 122014: 202015: 182016: 82017: 172018: 232019: 132020: 152021: 82022: 92023: 212024: 282025: 142026 (partial year): 5
2007high 35 (2007) · low 8 (2016)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MQV

57in 2025

2007: 144 days median2008: 102 days median2009: 180 days median2010: 147 days median2011: 92 days median2012: 107 days median2013: 197 days median2014: 153 days median2015: 184 days median2016: 214 days median2017: 124 days median2018: 124 days median2019: 90 days median2020: 132 days median2021: 88 days median2022: 118 days median2023: 74 days median2024: 55 days median2025: 57 days median2026 (partial year): 96 days median
2007high 214 (2016) · low 55 (2024)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · MQV

1in 2025

2007: 52008: 32009: 12011: 62012: 32013: 22016: 12017: 12018: 22020: 12023: 32024: 22025: 12026 (partial year): 4
2007high 6 (2011) · low 0 (2010)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · MQV

57in 2025

2007: 672008: 712009: 812010: 682011: 1142012: 1492013: 2232014: 1112015: 1252016: 1062017: 1072018: 862019: 652020: 1262021: 1012022: 472023: 1202024: 682025: 57
2007high 223 (2013) · low 47 (2022)2025

MAUDE reports naming product code MQV, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
200735144567
200832102371
200923180181
201017147068
201116926114
201291073149
2013121972223
2014201530111
2015181840125
201682141106
2017171241107
201823124286
20191390065
2020151321126
20218880101
20229118047
202321743120
20242855268
20251457157
20265964—

What is it indicated for?

TricOs T is indicated for use as a bone void filler for voids or gaps that are not intrinsic to the stability of the bony structure. It is indicated for surgically created osseous defects or osseous defects resulting from traumatic injury. TricOs T is a bone void filler without initial mechanical properties, therefore rigid fixation techniques may often be recommended. TricOs T is intended to be packed into bony voids or gaps of the skeletal system (i.e.…

Read the full statement (118 words)

TricOs T is indicated for use as a bone void filler for voids or gaps that are not intrinsic to the stability of the bony structure. It is indicated for surgically created osseous defects or osseous defects resulting from traumatic injury. TricOs T is a bone void filler without initial mechanical properties, therefore rigid fixation techniques may often be recommended.

TricOs T is intended to be packed into bony voids or gaps of the skeletal system (i.e. the extremities, spine, and pelvis). Following placement in the bony void or gap, TricOs T is resorbed and replaced with bone during the healing process.

Fibrin matrix without the HAfIACP granules is not indicated for use as a bone void filler.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K051722: Tricos T.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K051722

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026