Coral Spinal System
FDA 510(k) K041592 · Theken Surgical
510(k) numberK041592
Submission
- Device name
- Coral Spinal System
- Applicant
- Theken Surgical
Akron, OH, US - Received
- June 14, 2004
- Decision date
- September 16, 2004
- 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 |
More from K2m
| 510(k) | Device | Decision |
|---|---|---|
| K050058 | Theken Reveal VBR SystemMQP · Traditional | 05/17/2005SE |
| K032064 | Theken Cpod/Lpod Vertebral Body Replacement SystemMQP · Traditional | 02/20/2004SE |
| K012462 | Theken Large Cement RestrictorJDK · Traditional | 10/29/2001SESU |
| K012278 | Theken Small Cement RestrictorJDK · Traditional | 10/17/2001SESU |
| K010466 | Tether AcfsKWQ · Traditional | 05/16/2001SE |
| K994382 | Nonlinear Taper Lag ScrewHWC · Traditional | 03/10/2000SE |
| K994383 | Dogbone AcfsKWQ · Traditional | 02/04/2000SE |
| K983622 | Bodyform Thoraco-Lumbar Fixation SystemKWQ · Traditional | 12/30/1998SE |
Questions and answers
When was Coral Spinal System cleared by the FDA?
Coral Spinal System (K041592) received a 510(k) decision of Substantially Equivalent on September 16, 2004, 94 days after the submission was received.
What is the product code of K041592?
The FDA product code is KWP – Appliance, Fixation, Spinal Interlaminal, a Class II (moderate risk) device regulated under 21 CFR 888.3050.