K020853 is an FDA 510(k) clearance for the NUVASIVE MESH. This device is classified as a Mesh, Surgical, Metal (Class II - Special Controls, product code EZX).
Submitted by Nuvasive, Inc. (San Diego, US). The FDA issued a Cleared decision on June 13, 2002, 90 days after receiving the submission on March 15, 2002.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.3300.
| 510(k) Number | K020853 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 15, 2002 |
| Decision Date | June 13, 2002 |
| Days to Decision | 90 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | EZX — Mesh, Surgical, Metal |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.3300 |