3DMatrix Surgical Mesh
FDA 510(k) clearance K232602 · decided 2024-05-23
Clearance details
- K-number
- K232602
- Device name
- 3DMatrix Surgical Mesh
- Applicant
- Printbio, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2023-08-28
- Decision date
- 2024-05-23
- Days to decision
- 269 days
- Clearance type
- Traditional
- Product code
- OXF
- Device class
- 2
- Regulation number
- 878.3300
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Long Island City, NY, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| Restrata Soft Tissue Reinforcement (STR) (K251224) | Acera Surgical, Inc. | 2025-06-20 |
| 3DMatrix DynaFlex (DynaFlex) (K243302) | Printbio, Inc. | 2025-05-21 |
| GORE® ENFORM Biomaterial (K222919) | W. L. Gore and Associates, Inc. | 2022-12-19 |
| GORE ENFORM Biomaterial (K173333) | W. L. Gore & Associates, Inc. | 2018-04-05 |
| SERI Contour (K172545) | Sofregen Medical, Inc. | 2017-09-22 |
| GORE BIO-A Tissue Reinforcement (K163217) | W. L. Gore & Associates, Inc. | 2017-02-10 |
| SERI SURGICAL SCAFFOLD (K123128) | Allergan | 2013-04-25 |
Recalls involving this device
No recalls on record reference this clearance.