| Device Type ID | 5770 |
| Device Name | Staple, Implantable, Reprocessed |
| Regulation Description | Implantable Staple. |
| 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 | 878.4750 [🔎] |
| FDA Device Classification | Class 2 Medical Device |
| Product Code | NLL |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
| Device Type ID | 5770 |
| Device | Staple, Implantable, Reprocessed |
| Product Code | NLL |
| FDA Device Classification | Class 2 Medical Device |
| Regulation Description | Implantable Staple. |
| CFR Regulation Number | 878.4750 [🔎] |
| Device Problems | |
|---|---|
Positioning Failure | 1 |
Device Operates Differently Than Expected | 1 |
| Total Device Problems | 2 |