510(k) · Cleared
ClearedOSSIOfiber® Cannulated Trimmable Fixation Nail
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
OSSIO, Ltd. · HTY Pin, Fixation, Smooth
Cleared on Sep 13, 2023 as substantially equivalent to K203465 (OSSIO, Ltd., 2021) after a 180-day review. Its family tree reaches back 5 generations to 1990. 4 later devices descend from it.
- Decided
- Sep 13, 2023
- Review
- 180 days
- Class
- Class II
- Product code
- HTY
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 5 generations to K901456 (1990). 7 ancestors in all. 4 later devices descend from it, 1 citing it directly.
- Root · 5 generations backK901456 Orthosorb (R) Absorbable PinJohnson & Johnson International · 1990
- 4 generations backK031712 Inion Otps Biodegradable PinInion, Ltd. · 2003
- 3 generations backK050275 Modification to: Inion Otps Biodegradable PinInion, Ltd. · 2005
- 2 generations backK181180 OSSIO™ Pin Product FamilyOSSIO, Ltd. · 2019
- 1 generation backK203465 OSSIOfiber Cannulated Trimmable Fixation Nail, OSSIOfiber Trimmable…OSSIO, Ltd. · 2021
- This deviceK230750 OSSIOfiber® Cannulated Trimmable Fixation NailOSSIO, Ltd. · 2023
- Descendant · cites it directly · 3 of its ownK231272 OSSIOfiber® Pin Product Family, OSSIOfiber® Compression Screw…OSSIO, Ltd. · 2023
- Descendant · 2 generations on · 2 of its ownK233198 OSSIOfiber® Threaded Trimmable Fixation NailsOSSIO, Ltd. · 2024
- Descendant · 2 generations on · 1 of its ownK241277 OSSIOfiber® Threaded Trimmable Fixation NailOSSIO, Ltd. · 2024
- Descendant · 2 generations on · 0 of its ownK254077 OSSIOfiber® Threaded Trimmable Fixation NailOSSIO, Ltd. · 2026
Most influential descendants
Showing 4 of 4 · See all- 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
- K241277OSSIOfiber® Threaded Trimmable Fixation NailOSSIO, Ltd. · 2024 · 2 generations on1descendant
- K254077OSSIOfiber® Threaded Trimmable Fixation NailOSSIO, Ltd. · 2026 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −5 | K901456 | Orthosorb (R) Absorbable Pin | Johnson & Johnson International | 1990 | — |
| −4 | K031712 | Inion Otps Biodegradable Pin | Inion, Ltd. | 2003 | — |
| −3 | K050275 | Modification to: Inion Otps Biodegradable Pin | Inion, Ltd. | 2005 | — |
| −2 | K181180 | OSSIO™ Pin Product Family | OSSIO, Ltd. | 2019 | — |
| −1 | K203465 | OSSIOfiber Cannulated Trimmable Fixation Nail, OSSIOfiber Trimmable Fixation… | OSSIO, Ltd. | 2021 | — |
| 0 (this device) | K230750 | OSSIOfiber® Cannulated Trimmable Fixation Nail | OSSIO, Ltd. | 2023 | — |
| +1 | K231272 | OSSIOfiber® Pin Product Family, OSSIOfiber® Compression Screw, OSSIOfiber®… | OSSIO, Ltd. | 2023 | — |
| +2 | K233198 | OSSIOfiber® Threaded Trimmable Fixation Nails | OSSIO, Ltd. | 2024 | — |
| +2 | K241277 | OSSIOfiber® Threaded Trimmable Fixation Nail | OSSIO, Ltd. | 2024 | — |
| +2 | K254077 | OSSIOfiber® Threaded Trimmable Fixation Nail | OSSIO, Ltd. | 2026 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1997 | 1 | 0 |
| 2001 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2023 | 1 | 0 |
| 2024 | 2 | 0 |
| 2026 | 1 | 0 |
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 K231272 OSSIOfiber® Pin Product Family, OSSIOfiber®…score 19.3 · 14 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the 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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K203465 | OSSIOfiber Cannulated Trimmable Fixation Nail, OSSIOfiber Trimmable Fixation Nail…Summary page 4…c bone fixation fastener Regulatory Class: Class II, 21 C.F.R. § 888.3040 Product Code: HTY Predicate Devices OSSIOfiber® Cannulated Trimmable Fixation Nail (K203465) Reference Devices Arthrex Bio-pin (K050259) OSSIOfiber® Compression Screw, 6.5mm (K221193)… | 2021 |
| † | K050259 | Arthrex Bio-Pin | 2005 |
| † | K221193 | OSSIOfiber Compression Screw, OSSIOfiber Compression Screw, 6.5mm | 2022 |
| † | K181180 | OSSIO™ Pin Product Family | 2019 |
What descends from it? (4)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K231272 | OSSIOfiber® Pin Product Family, OSSIOfiber® Compression Screw, OSSIOfiber® Trimmable… | 2023 | 3 |
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 33 years and passes through 3 companies; a new generation was cleared every 2.7 years on median.
- None of the 7 ancestors has a recall.
- Of its descendants, K231272 (OSSIO, Ltd., 2023) has gone furthest, with 3 descendants of its own.
- 2 other devices also cite its predicate K203465.
How does its category compare?
All HTY devicesHTY Pin, Fixation, Smooth: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.
FDA decisions per year · HTY
5in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · HTY
90in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · HTY
2in 2022
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · HTY
39in 2025
MAUDE reports naming product code HTY, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 6 | 112 | 0 | 46 |
| 2008 | 6 | 86 | 0 | 38 |
| 2009 | 2 | — | 1 | 36 |
| 2010 | 9 | 180 | 1 | 33 |
| 2011 | 6 | 82 | 0 | 164 |
| 2012 | 4 | 76 | 0 | 129 |
| 2013 | 4 | 128 | 0 | 187 |
| 2014 | 8 | 73 | 0 | 149 |
| 2015 | 8 | 101 | 0 | 121 |
| 2016 | 6 | 114 | 2 | 128 |
| 2017 | 5 | 127 | 0 | 82 |
| 2018 | 4 | 162 | 0 | 138 |
| 2019 | 4 | 93 | 1 | 222 |
| 2020 | 5 | 108 | 0 | 210 |
| 2021 | 5 | 137 | 0 | 148 |
| 2022 | 4 | 121 | 2 | 96 |
| 2023 | 5 | 146 | 0 | 153 |
| 2024 | 1 | — | 0 | 297 |
| 2025 | 5 | 90 | 0 | 39 |
| 2026 | 2 | — | 1 | — |
What is it indicated for?
OSSIOfiber® Cannulated Trimmable Fixation Nails are 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 as stated in the FDA summary.
https://510kreport.com/device/K230750 · printed Nov 6, 2026
Cite this page
510(k) Report. “K230750: OSSIOfiber® Cannulated Trimmable Fixation Nail.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K230750
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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