Definition: For Reinforcement Of Soft Tissue Where Weakness Exists In Abdominal Wall Defects.
Device Type ID | 5848 |
Device Name | Mesh, Surgical, Non-absorbable, Large Abdominal Wall Defects |
Physical State | A Non-absorbable Mesh; Either Square, Round, Rectangular Or Of Various Other Shapes |
Technical Method | A Non-absorbable Mesh That Reinforces Soft Tissue |
Target Area | Abdominal Wall |
Regulation Description | Surgical Mesh. |
Regulation Medical Specialty | General & Plastic Surgery |
Review Panel | General & Plastic Surgery |
Premarket Review | Office Of Device Evaluation (ODE) Division Of Surgical Devices (DSD) Plastic And Reconstructive Surgery Devices Branch Two - Skin/Wound Dressing/Aesthetic Injectables (PRSB2) |
Submission Type | 510(k) |
CFR Regulation Number | 878.3300 [🔎] |
FDA Device Classification | Class 2 Medical Device |
Product Code | OXJ |
GMP Exempt | No |
Summary MR | Eligible |
Implanted Device | Yes |
Life Support Device | No |
Third Party Review | Not Third Party Eligible |
Device Type ID | 5848 |
Device | Mesh, Surgical, Non-absorbable, Large Abdominal Wall Defects |
Product Code | OXJ |
FDA Device Classification | Class 2 Medical Device |
Regulation Description | Surgical Mesh. |
CFR Regulation Number | 878.3300 [🔎] |
Premarket Reviews | ||
---|---|---|
Manufacturer | Decision | |
MOLNLYCKE HEALTH CARE | ||
SUBSTANTIALLY EQUIVALENT | 1 | |
MOLNLYCKE HEALTH CARE US LLC | ||
SUBSTANTIALLY EQUIVALENT | 1 | |
MOLNLYCKE HEALTH CARE US, LLC | ||
SUBSTANTIALLY EQUIVALENT | 1 |
Device Problems | |
---|---|
Contamination During Use | 3 |
Adverse Event Without Identified Device Or Use Problem | 1 |
Device Dislodged Or Dislocated | 1 |
Hole In Material | 1 |
Microbial Contamination Of Device | 1 |
Total Device Problems | 7 |