510(k) Report

510(k) · Cleared

Cleared

OSSIO™ Pin Product Family

K181180510(k) TraditionalCleared Jan 10, 2019253-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

OSSIO, Ltd. · HTY Pin, Fixation, Smooth

Cleared on Jan 10, 2019 as substantially equivalent to K050275 (Inion, Ltd., 2005) after a 253-day review. Its family tree reaches back 3 generations to 1990. 13 later devices descend from it.

Decided
Jan 10, 2019
Review
253 days
Class
Class II
Product code
HTY
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K901456 (1990). 5 ancestors in all. 13 later devices descend from it, 5 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2001: 1 other ancestor1997: 1 other ancestor2023: 2 descendants cleared2022: 1 descendant cleared2020: 2 descendants cleared2025: 2 descendants cleared2021: 1 descendant cleared2024: 2 descendants cleared2026: 3 descendants clearedReference device: K133932 · Inion Freedompin · Inion OY · 2014Reference device: K071199 · Bonalive Granules · Vivoxid, Ltd. · 2008Reference device: K143660 · Milagro / Milagro Advance Interference Screw · Depuy Mitek, A Johnson & Johnson Company · 2015K901456 · Orthosorb (R) Absorbable Pin · Johnson & Johnson International · 1990K031712 · Inion Otps Biodegradable Pin · Inion, Ltd. · 2003K050275 · Modification to: Inion Otps Biodegradable Pin · Inion, Ltd. · 20051990200020102020
Other ancestors, by generationDescendants, by generation 3 generations back: 2 other ancestors 1 generation forward: 5 descendants2 generations forward: 7 descendants3 generations forward: 1 descendant K050275 · Modification to: Inion Otps Biodegradable Pin · Inion, Ltd. · 2005K031712 · Inion Otps Biodegradable Pin · Inion, Ltd. · 2003K901456 · Orthosorb (R) Absorbable Pin · Johnson & Johnson International · 19900
  1. Root · 3 generations backK901456 Orthosorb (R) Absorbable PinJohnson & Johnson International · 1990
  2. 2 generations backK031712 Inion Otps Biodegradable PinInion, Ltd. · 2003
  3. 1 generation backK050275 Modification to: Inion Otps Biodegradable PinInion, Ltd. · 2005
  4. This deviceK181180 OSSIO™ Pin Product FamilyOSSIO, Ltd. · 2019
  5. Descendant · cites it directly · 5 of its ownK203465 OSSIOfiber Cannulated Trimmable Fixation Nail, OSSIOfiber Trimmable…OSSIO, Ltd. · 2021
  6. Descendant · 2 generations on · 4 of its ownK230750 OSSIOfiber® Cannulated Trimmable Fixation NailOSSIO, Ltd. · 2023
  7. Descendant · cites it directly · 3 of its ownK250646 Impact PEEK Union Nail SystemNvision Biomedical Technologies · 2025
  8. Descendant · cites it directly · 3 of its ownK231272 OSSIOfiber® Pin Product Family, OSSIOfiber® Compression Screw…OSSIO, Ltd. · 2023
  9. Descendant · 2 generations on · 2 of its ownK233198 OSSIOfiber® Threaded Trimmable Fixation NailsOSSIO, Ltd. · 2024

Showing 5 of 13 descendants. See all descendants

Descendants cleared per year

2020: 22021: 12022: 12023: 22024: 22025: 22026: 3
2020high 3 (2026) · low 1 (2021)2026

Most influential descendants

Showing 5 of 13 · See all
  • K203465OSSIOfiber Cannulated Trimmable Fixation Nail, OSSIOfiber Trimmable Fixation Nail…OSSIO, Ltd. · 2021 · cites it directly5descendants
  • K230750OSSIOfiber® Cannulated Trimmable Fixation NailOSSIO, Ltd. · 2023 · 2 generations on4descendants
  • K250646Impact PEEK Union Nail SystemNvision Biomedical Technologies · 2025 · cites it directly3descendants
  • K231272OSSIOfiber® Pin Product Family, OSSIOfiber® Compression Screw, OSSIOfiber® Trimmable…OSSIO, Ltd. · 2023 · cites it directly3descendants
  • K233198OSSIOfiber® Threaded Trimmable Fixation NailsOSSIO, Ltd. · 2024 · 2 generations on2descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K901456Orthosorb (R) Absorbable PinJohnson & Johnson International1990—
−2K031712Inion Otps Biodegradable PinInion, Ltd.2003—
−1K050275Modification to: Inion Otps Biodegradable PinInion, Ltd.2005—
0 (this device)K181180OSSIO™ Pin Product FamilyOSSIO, Ltd.2019—
+1K203465OSSIOfiber Cannulated Trimmable Fixation Nail, OSSIOfiber Trimmable Fixation…OSSIO, Ltd.2021—
+2K230750OSSIOfiber® Cannulated Trimmable Fixation NailOSSIO, Ltd.2023—
+1K250646Impact PEEK Union Nail SystemNvision Biomedical Technologies2025—
+1K231272OSSIOfiber® Pin Product Family, OSSIOfiber® Compression Screw, OSSIOfiber®…OSSIO, Ltd.2023—
+2K233198OSSIOfiber® Threaded Trimmable Fixation NailsOSSIO, Ltd.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199710
200110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202020
202110
202210
202320
202420
202520
202630
FIG. 1 — Lineage of K181180, 1990–2026Source: 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
Get a 510(k) Report

What was it cleared against? (1)

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
*K050275Modification to: Inion Otps Biodegradable Pin
Summary page 4
…or threaded metallic bone fixation fastener Regulatory Class: Class II, 21 C.F.R. § 888.3040 Product Code: HTY Predicate Devices Inion OTPSTM Biodegradable Pin (K050275) Reference Devices Inion FreedomPinTM, (K133932) BonAlive Biomaterials Ltd., BonAlive® granules, (K071199) D…
Inion, Ltd.2005—
†K133932Inion FreedompinInion OY2014—
†K071199Bonalive GranulesVivoxid, Ltd.2008—
†K143660Milagro / Milagro Advance Interference ScrewDepuy Mitek, A Johnson & Johnson Company2015—

Also cleared against K050275: 2 other devices →

What descends from it? (13)

See all 13

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

NumberDeviceApplicantDecidedDescendants
K203465OSSIOfiber Cannulated Trimmable Fixation Nail, OSSIOfiber Trimmable Fixation Nail…OSSIO, Ltd.20215
K250646Impact PEEK Union Nail SystemNvision Biomedical Technologies20253
K231272OSSIOfiber® Pin Product Family, OSSIOfiber® Compression Screw, OSSIOfiber® Trimmable…OSSIO, Ltd.20233
K190652OSSIOfiber™ Hammertoe Fixation System/OSSIOfiber™ Hammertoe Fixation ImplantOSSIO, Ltd.20201
K211789restor3d Pin ImplantsRestor3D20220

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 29 years and passes through 3 companies; a new generation was cleared every 13.0 years on median.
  • None of the 5 ancestors has a recall.
  • Of its descendants, K203465 (OSSIO, Ltd., 2021) has gone furthest, with 5 descendants of its own.
  • 2 other devices also cite its predicate K050275.

How does its category compare?

All HTY devices

HTY Pin, Fixation, Smooth: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, 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 OSSIO™ Pin Product Family is indicated for maintenance of alignment and fixation of bone fractures, osteotomies, arthrodesis, and bone grafts in the presence of appropriate additional immobilization (e.g. rigid fixation implants, cast, brace).

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K181180: OSSIO™ Pin Product Family.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K181180

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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