The following data is part of a premarket notification filed by Osteonics Corp. with the FDA for Osteo Austin Moore Endoprosthesis System.
| Device ID | K974807 |
| 510k Number | K974807 |
| Device Name: | OSTEO AUSTIN MOORE ENDOPROSTHESIS SYSTEM |
| Classification | Prosthesis, Hip, Hemi-, Femoral, Metal |
| Applicant | OSTEONICS CORP. 59 ROUTE 17 Allendale, NJ 07401 -1677 |
| Contact | Terry Sheridan |
| Correspondent | Terry Sheridan OSTEONICS CORP. 59 ROUTE 17 Allendale, NJ 07401 -1677 |
| Product Code | KWL |
| CFR Regulation Number | 888.3360 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-12-23 |
| Decision Date | 1998-03-16 |
| Summary: | summary |