Mitek Rapidloc-Pds Meniscal Repair System
FDA 510(k) K023388 · Mitek Worldwide
510(k) numberK023388
Submission
- Device name
- Mitek Rapidloc-Pds Meniscal Repair System
- Applicant
- Mitek Worldwide
Norwood, MA, US - Received
- October 9, 2002
- Decision date
- December 27, 2002
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary 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
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|---|---|---|---|
| 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 |
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| K032078 | Mitek Micro QuickanchorNOV · Traditional | 08/25/2003SE |
| K030995 | Minilok Quickanchor PlusHWC · Traditional | 06/26/2003SE |
| K031519 | Cufflok AnchorMAI · Special | 06/06/2003SE |
| K031406 | Exojet Tissue Management SystemHRX · Traditional | 05/30/2003SE |
| K024115 | Microfix Quickanchor PlusHWC · Traditional | 03/13/2003SE |
| K021953 | Mitek Pds/Pga StapleJDR · Traditional | 12/20/2002SE |
| K021883 | Biofastin RC Threaded Suture AnchorHWC · Special | 07/01/2002SE |
Questions and answers
When was Mitek Rapidloc-Pds Meniscal Repair System cleared by the FDA?
Mitek Rapidloc-Pds Meniscal Repair System (K023388) received a 510(k) decision of Substantially Equivalent on December 27, 2002, 79 days after the submission was received.
What is the product code of K023388?
The FDA product code is JDR – Staple, Fixation, Bone, a Class II (moderate risk) device regulated under 21 CFR 888.3030.