510(k) Report

510(k) · Cleared

Cleared

Osteotrans-OT Pin

K073311510(k) TraditionalCleared May 13, 2008172-day reviewClass II21 CFR 888.3040

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

Takiron Co., Ltd. · HTY Pin, Fixation, Smooth

Cleared on May 13, 2008 as substantially equivalent to K041288 (Linvatec Biomaterials, Inc., 2004) and 2 other predicates after a 172-day review. Its family tree reaches back 6 generations to 1987.

Decided
May 13, 2008
Review
172 days
Class
Class II
Product code
HTY
Recalls
None
Predicates
3

Its longest line of descent runs back 6 generations to K864912 (1987). 13 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 6 generations backK864912 PDS (Polydioxanon) Absorbable PinJohnson & Johnson Professionals, Inc. · 1987
  2. 5 generations backK993074 Smart Nail Models 521516, 521520,521525, 531516, 531520. 531525Bionx Implants, Ltd. · 1999
  3. 4 generations backK012000 1.5MM Bone Fixation KitBionx Implants, Ltd. · 2001
  4. 3 generations backK013546 Modification to: 1.5 Bone Fixation Kit, Models BXS6114, BXS6214Bionx Implants, Inc. · 2001
  5. 2 generations backK031981 2.4 Smartnail, Models 532416, 532425, 532435, 532445Linvatec Biomaterials, Ltd. · 2003
  6. 1 generation backK041288 Modification to SmartpinLinvatec Biomaterials, Inc. · 2004
  7. This deviceK073311 Osteotrans-OT PinTakiron Co., Ltd. · 2008
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K864912PDS (Polydioxanon) Absorbable PinJohnson & Johnson Professionals, Inc.1987—
−5K993074Smart Nail Models 521516, 521520,521525, 531516, 531520. 531525Bionx Implants, Ltd.1999—
−4K0120001.5MM Bone Fixation KitBionx Implants, Ltd.2001—
−3K013546Modification to: 1.5 Bone Fixation Kit, Models BXS6114, BXS6214Bionx Implants, Inc.2001—
−2K0319812.4 Smartnail, Models 532416, 532425, 532435, 532445Linvatec Biomaterials, Ltd.2003—
−1K041288Modification to SmartpinLinvatec Biomaterials, Inc.2004—
0 (this device)K073311Osteotrans-OT PinTakiron Co., Ltd.2008—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198910
199010
199410
199710
200120
200310
FIG. 1 — Lineage of K073311, 1987–2008Source: 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 HTY? 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 HTY device

  1. #1 K231272 OSSIOfiber® Pin Product Family, OSSIOfiber®…score 19.3 · 14 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (3)

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
*K041288Modification to Smartpin
Summary page 1
…tion Number: Takiron Co., Ltd. has not yet obtained an Establishment Registration Number. Legally Marketed Predicate Devices: 1. Linvatec Biomaterials Ltd.; SmartPin (K041288) 2. Inion Ltd.; Inion OTPSTM Biodegradable Pin (K031712) 3. Bionx Implants Ltd.; PLLA Pin (K010983) Intended Use: The OSTEOT…
Linvatec Biomaterials, Inc.2004—
*K031712Inion Otps Biodegradable Pin
Summary page 1
…ablishment Registration Number. Legally Marketed Predicate Devices: 1. Linvatec Biomaterials Ltd.; SmartPin (K041288) 2. Inion Ltd.; Inion OTPSTM Biodegradable Pin (K031712) 3. Bionx Implants Ltd.; PLLA Pin (K010983) Intended Use: The OSTEOTRANS"m-OT Pin is intended for fixation of fragments of fra…
Inion, Ltd.2003—
*K010983Plla Pin
Summary page 1
…eted Predicate Devices: 1. Linvatec Biomaterials Ltd.; SmartPin (K041288) 2. Inion Ltd.; Inion OTPSTM Biodegradable Pin (K031712) 3. Bionx Implants Ltd.; PLLA Pin (K010983) Intended Use: The OSTEOTRANS"m-OT Pin is intended for fixation of fragments of fractured non-load bearing bones, osteotomies an…
Bionx Implants, Inc.2001—

Also cleared against K041288: 1 other device →

What descends from it?

No later submission names this one as a predicate yet.

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 21 years and passes through 6 companies; a new generation was cleared every 1.7 years on median.
  • None of the 13 ancestors has a recall.
  • 1 other device also cites its predicate K041288.

How does its category compare?

All HTY devices

HTY Pin, Fixation, Smooth: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.

FDA decisions per year · HTY

5in 2025

2007: 62008: 62009: 22010: 92011: 62012: 42013: 42014: 82015: 82016: 62017: 52018: 42019: 42020: 52021: 52022: 42023: 52024: 12025: 52026 (partial year): 2
2007high 9 (2010) · low 1 (2024)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HTY

90in 2025

2007: 112 days median2008: 86 days median2010: 180 days median2011: 82 days median2012: 76 days median2013: 128 days median2014: 73 days median2015: 101 days median2016: 114 days median2017: 127 days median2018: 162 days median2019: 93 days median2020: 108 days median2021: 137 days median2022: 121 days median2023: 146 days median2025: 90 days median
2007high 180 (2010) · low 73 (2014)2026

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

Recalls per year · HTY

2in 2022

2009: 12010: 12016: 22019: 12022: 22026 (partial year): 1
2007high 2 (2016) · low 0 (2007)2026

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

Adverse event reports per year · HTY

39in 2025

2007: 462008: 382009: 362010: 332011: 1642012: 1292013: 1872014: 1492015: 1212016: 1282017: 822018: 1382019: 2222020: 2102021: 1482022: 962023: 1532024: 2972025: 39
2007high 297 (2024) · low 33 (2010)2025

MAUDE reports naming product code HTY, 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
20076112046
2008686038
20092—136
20109180133
20116820164
20124760129
201341280187
20148730149
201581010121
201661142128
20175127082
201841620138
20194931222
202051080210
202151370148
20224121296
202351460153
20241—0297
2025590039
20262—1—

What is it indicated for?

The OSTEOTRANSm-OT Pin is intended for fixation of fragments of fractured

non-load bearing bones, osteotomies and arthrodeses or bone grafts, for example in the

fixation of apical fragments and cancellous/non-load bearing fragments in the presence

of appropriate immobilization.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K073311: Osteotrans-OT Pin.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K073311

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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