SCS DT-02 Transverse Connector
FDA 510(k) K003823 · Ortho Tec, LLC
510(k) numberK003823
Submission
- Device name
- SCS DT-02 Transverse Connector
- Applicant
- Ortho Tec, LLC
Beverly Hills, CA, US - Received
- December 11, 2000
- Decision date
- July 11, 2001
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- KWP – Appliance, Fixation, Spinal Interlaminal
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3050
- Specialty
- Orthopedic
- Implant
- Yes
Other 510(k)s with product code KWP
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K143278 | LnK Posterior Cervical Fixation SystemKWP · Traditional | L&K BIOMED Co., Ltd. | 07/29/2015SE |
| K150753 | OASYS SystemKWP · Traditional | Stryker Corporation | 06/09/2015SE |
| K150851 | Sure Lok Mini Posterior Cervical/Upper Thoracic SystemKWP · Special | Precision Spine, Inc. | 06/04/2015SE |
| K142867 | Reliance Posterior Cervical-Thoracic SystemKWP · Special | Reliance Medical Systems, LLC | 04/29/2015SE |
| K150254 | Streamline OCT Occipito-Cervico-Thoracic SystemKWP · Traditional | Pioneer Surgical Technology, Inc. (Dba Rti… | 04/28/2015SE |
| K142253 | SOLSTICE OCT SystemKWP · Traditional | Life Spine, Inc. | 04/23/2015SE |
| K150229 | SOLSTICE OCT SystemKWP · Traditional | Life Spine, Inc. | 04/07/2015SE |
| K143249 | SOLSTICE OCT SystemKWP · Traditional | Life Spine, Inc. | 04/07/2015SE |
| K142741 | OASYS SystemKWP · Traditional | Stryker Corporation | 01/15/2015SE |
| K142558 | Caspian OCT/MESA Mini/DENALI Mini Spinal SystemKWP · Special | K2m | 12/22/2014SE |
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| K040514 | Eovia Calcium Phosphate CeramicMQV · Traditional | 05/03/2004SE |
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| K030958 | Oria Spinal System, Domino and Tube ConnectorsMNI · Traditional | 11/20/2003SE |
| K031471 | Oria Spinal Clip System, Lateral Intermediate Connector, Model AL01KWP · Traditional | 10/10/2003SE |
| K023884 | Modification Oria Spinal SystemKWP · Traditional | 08/20/2003SE |
| K023378 | Oria ClarisMNH · Traditional | 06/27/2003SE |
| K031452 | Oria Spinal Clip System, Sacral Connector, Models CA03 and AO03KWP · Special | 06/18/2003SE |
| K030500 | Oria ZenithKWQ · Special | 03/20/2003SE |
| K023377 | Oria Cervical PlatesKWQ · Traditional | 03/04/2003SE |
| K030253 | Oria Spinal Clip System, Lengthened Lateral Connector, Model AL06KWP · Special | 02/21/2003SE |
Questions and answers
When was SCS DT-02 Transverse Connector cleared by the FDA?
SCS DT-02 Transverse Connector (K003823) received a 510(k) decision of Substantially Equivalent on July 11, 2001, 212 days after the submission was received.
What is the product code of K003823?
The FDA product code is KWP – Appliance, Fixation, Spinal Interlaminal, a Class II (moderate risk) device regulated under 21 CFR 888.3050.