Osteotrans-Ot Pin
FDA 510(k) K073311 · Takiron Co., Ltd.
510(k) numberK073311
Submission
- Device name
- Osteotrans-Ot Pin
- Applicant
- Takiron Co., Ltd.
Chuo-Ku, Kobe, Hyogo, JP - Received
- November 23, 2007
- Decision date
- May 13, 2008
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- HTY – Pin, Fixation, Smooth
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3040
- Specialty
- Orthopedic
- Implant
- Yes
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| K253325 | ZipToe Hammertoe Fusion SystemHTY · Traditional | Toetal Solutions | 12/29/2025SE |
| K252657 | Impact PEEK Union Nail SystemHTY · Special | Nvision Biomedical Technologies, Inc. | 09/19/2025SE |
| K250315 | Ronavis FX (FX-001)HTY · Traditional | AIRS, Inc. | 08/01/2025SE |
| K251362 | PediFlex Flexible Nail SystemHTY · Traditional | OrthoPediatrics Corp. | 06/24/2025SE |
| K250646 | Impact PEEK Union Nail SystemHTY · Traditional | Nvision Biomedical Technologies | 06/11/2025SE |
| K241014 | Biomet Kirschner Wires (K-Wires)HTY · Traditional | Biomet, Inc. | 05/22/2024SE |
| K231272 | OSSIOfiber® Pin Product Family, OSSIOfiber® Compression Screw, OSSIOfiber® Trimmable…HTY · Traditional | OSSIO , Ltd. | 12/01/2023SE |
| K231147 | Hammerdesis Interphalangeal Fusion SystemHTY · Traditional | Intelivation | 09/14/2023SE |
| K230750 | OSSIOfiber® Cannulated Trimmable Fixation NailHTY · Traditional | OSSIO , Ltd. | 09/13/2023SE |
More from OSSIO , Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K081390 | Bioactif Osteotrans Interfence ScrewHWC · Traditional | 08/12/2008SE |
| K073006 | Osteotrans -Mx Bioabsorbable Bone Fixation SystemGWO · Traditional | 05/29/2008SE |
| K073312 | Osteotrans-Ot ScrewHWC · Traditional | 05/13/2008SE |
| K062691 | ComporusMQV · Traditional | 04/15/2008SE |
| K061881 | Osteotrans -Mx Bioabsorbable Bone Fixation SystemJEY · Traditional | 03/14/2007SE |
Questions and answers
When was Osteotrans-Ot Pin cleared by the FDA?
Osteotrans-Ot Pin (K073311) received a 510(k) decision of Substantially Equivalent on May 13, 2008, 172 days after the submission was received.
What is the product code of K073311?
The FDA product code is HTY – Pin, Fixation, Smooth, a Class II (moderate risk) device regulated under 21 CFR 888.3040.