3DMatrix Surgical Mesh— 510(k) K232602
Substantially EquivalentPrintbio, Inc.
FDA 510(k) clearance K232602 for 3DMatrix Surgical Mesh, Substantially Equivalent on 2024-05-23. Applicant: Printbio, Inc.. Device class: 2.
Clearance details
- Applicant
- Printbio, Inc.
- Product code
- Code OXF
- Device class
- Class 2
- Regulation
- 21 CFR 878.3300
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Long Island City, NY, US
Recent devices under product code OXF
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