K232602 is an FDA 510(k) clearance for the 3DMatrix Surgical Mesh. This device is classified as a Mesh, Surgical, Absorbable, Plastic And Reconstructive Surgery (Class II - Special Controls, product code OXF).
Submitted by Printbio, Inc. (Long Island City, US). The FDA issued a Cleared decision on May 23, 2024, 269 days after receiving the submission on August 28, 2023.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.3300. For Reinforcement Of Soft Tissue Where Weakness Exists In Plastic And Reconstructive Surgery..
| 510(k) Number | K232602 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 28, 2023 |
| Decision Date | May 23, 2024 |
| Days to Decision | 269 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | OXF — Mesh, Surgical, Absorbable, Plastic And Reconstructive Surgery |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.3300 |
| Definition | For Reinforcement Of Soft Tissue Where Weakness Exists In Plastic And Reconstructive Surgery. |