Lotus
FDA 510(k) K131427 · Spinal Elements, Inc.
510(k) numberK131427
Submission
- Device name
- Lotus
- Applicant
- Spinal Elements, Inc.
Carlsbad, CA, US - Received
- May 17, 2013
- Decision date
- October 24, 2013
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 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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| K250773 | Luna® Ti Interbody Fusion SystemMAX · Traditional | 02/04/2026SE |
| K242527 | The Karma® Fixation SystemMRW · Traditional | 05/21/2025SE |
| K243916 | Primus Spinal Fixation SystemNKB · Traditional | 02/21/2025SE |
| K234150 | Lucent® XPMAX · Traditional | 03/27/2024SE |
| K231593 | Sapphire X3 Anterior Cervical Plate SystemKWQ · Traditional | 08/02/2023SE |
| K231252 | Ventana L Spinal SystemMAX · Traditional | 06/30/2023SE |
| K222833 | Ventana C Spinal SystemODP · Traditional | 05/19/2023SE |
| K222516 | Mercury® II Spinal SystemNKB · Traditional | 12/01/2022SE |
Questions and answers
When was Lotus cleared by the FDA?
Lotus (K131427) received a 510(k) decision of Substantially Equivalent on October 24, 2013, 160 days after the submission was received.
What is the product code of K131427?
The FDA product code is KWP – Appliance, Fixation, Spinal Interlaminal, a Class II (moderate risk) device regulated under 21 CFR 888.3050.