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 |