Submission Details
| 510(k) Number | K240592 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | March 01, 2024 |
| Decision Date | May 24, 2024 |
| Days to Decision | 84 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | Summary PDF |
K240592 is an FDA 510(k) clearance for the Wolff's Law Anterior Cervical Plate System, a Appliance, Fixation, Spinal Intervertebral Body (Class II — Special Controls, product code KWQ), submitted by Spinal Simplicity, LLC (Overland Park, US). The FDA issued a Cleared decision on May 24, 2024, 84 days after receiving the submission on March 1, 2024. This device falls under the Orthopedic review panel. Regulated under 21 CFR 888.3060.
| 510(k) Number | K240592 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | March 01, 2024 |
| Decision Date | May 24, 2024 |
| Days to Decision | 84 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | Summary PDF |
| Product Code | KWQ — Appliance, Fixation, Spinal Intervertebral Body |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 888.3060 |