The following data is part of a premarket notification filed by Fournitures Hospitalieres Industrie with the FDA for Arrow Reverse Porous Glenoid.
| Device ID | K171789 |
| 510k Number | K171789 |
| Device Name: | ARROW Reverse Porous Glenoid |
| Classification | Shoulder Prosthesis, Reverse Configuration |
| Applicant | Fournitures Hospitalieres Industrie ZI De Kernevez - 6 Rue Nobel Quimper, FR 29000 |
| Contact | Patricia Donnard |
| Correspondent | Patricia Donnard Fournitures Hospitalieres Industrie ZI De Kernevez - 6 Rue Nobel Quimper, FR 29000 |
| Product Code | PHX |
| Subsequent Product Code | KWS |
| Subsequent Product Code | KWT |
| CFR Regulation Number | 888.3660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-06-15 |
| Decision Date | 2018-01-23 |
| Summary: | summary |