| Device |
shoulder arthroplasty implantation system |
| Regulation Description |
Shoulder joint metal/polymer semi-constrained cemented prosthesis. |
| Definition |
Intended to be used to assist in the implantation of a specific shoulder arthroplasty device or a set of specific shoulder arthroplasty devices. Indicated to include guiding alignment, making or establishing cuts, selecting, sizing, attaching, positioning or orienting implant components. |
| Physical State |
A device accessory or set of device accessories |
| Technical Method |
Aids the surgeon in performing the implantation of the shoulder implant |
| Target Area |
Shoulder |
| Regulation Medical Specialty |
Orthopedic |
| Review Panel |
Orthopedic |
| Product Code | QHE |
| Premarket Review |
Joint Arthroplasty Devices
(DHT6A)
Joint Arthroplasty Devices
(DHT6A)
|
| Submission Type |
510(k)
|
| Regulation Number |
888.3660
|
| Device Class |
2
|
| Total Product Life Cycle (TPLC) |
TPLC Product Code Report
|
| GMP Exempt? |
No
|
Summary Malfunction Reporting |
Ineligible |
| Implanted Device? |
No
|
| Life-Sustain/Support Device? |
No
|
| Third Party Review |
Not Third Party Eligible |