LMT Bone Anchor
FDA 510(k) K953764 · Li Medical Technologies, Inc.
510(k) numberK953764
Submission
- Device name
- LMT Bone Anchor
- Applicant
- Li Medical Technologies, Inc.
Shelton, CT, US - Received
- August 11, 1995
- Decision date
- August 25, 1995
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- JDR – Staple, Fixation, Bone
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3030
- Specialty
- Orthopedic
- Implant
- Yes
Other 510(k)s with product code JDR
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K262451 | Arthrex DynaNite StaplesJDR · Traditional | Arthrex, Inc. | 09/01/2026SE |
| K261121 | Megalodon Dynamic Compression SystemJDR · Traditional | Paragon 28, Inc. | 08/06/2026SE |
| K250712 | Linkt Compression Staple SystemJDR · Traditional | Trax Surgical | 05/14/2025SE |
| K243888 | Medline UNITE® REFLEX® Hybrid Nitinol Implant SystemJDR · Traditional | Medline Industries, LP | 04/11/2025SE |
| K243742 | Arthrex DynaNite Nitinol StaplesJDR · Traditional | Arthrex, Inc. | 01/31/2025SE |
| K243658 | TMC Compression Implant SystemJDR · Special | Treace Medical Concepts | 12/26/2024SE |
| K242415 | TMC Compression Implant SystemJDR · Special | Treace Medical Concepts | 09/06/2024SE |
| K240212 | COGNiTiON Staple SystemJDR · Special | Ortho Solutions UK , Ltd. | 02/23/2024SE |
| K232990 | ATOMIC Nitinol Fixation SystemJDR · Traditional | Rmr Ortho, LLC | 01/12/2024SE |
| K230724 | arcad® 2.0 Duo & Quadro osteosynthesis compressive staplesJDR · Traditional | Novastep | 12/04/2023SE |
More from Novastep
| 510(k) | Device | Decision |
|---|---|---|
| K002413 | Ultrasorb Suture AnchorMAI · Traditional | 09/19/2000SE |
| K993373 | Rotorblade Suture AnchorMAI · Special | 10/27/1999SE |
| K992938 | Rotorblade Suture AnchorMAI · Special | 09/23/1999SE |
| K983435 | RotorbladeMAI · Abbreviated | 04/29/1999SE |
| K981764 | LM AnchorMBI · Abbreviated | 07/13/1998SE |
| K981755 | LM AnchorMBI · Abbreviated | 07/13/1998SE |
| K963288 | LM Bone AnchorMBI · Traditional | 11/13/1996SE |
| K963812 | LM Bone Anchor (Orthopedics)MBI · Traditional | 11/12/1996SE |
| K960825 | LM Anchor or Other Proprietary NameMBI · Traditional | 04/30/1996SE |
| K960439 | LM Bone AnchorMBI · Traditional | 04/18/1996SE |
Questions and answers
When was LMT Bone Anchor cleared by the FDA?
LMT Bone Anchor (K953764) received a 510(k) decision of Substantially Equivalent on August 25, 1995, 14 days after the submission was received.
What is the product code of K953764?
The FDA product code is JDR – Staple, Fixation, Bone, a Class II (moderate risk) device regulated under 21 CFR 888.3030.