The following data is part of a premarket notification filed by Smith & Nephew Richards, Inc. with the FDA for Hapex Incus.
| Device ID | K950887 |
| 510k Number | K950887 |
| Device Name: | HAPEX INCUS |
| Classification | Prosthesis, Partial Ossicular Replacement |
| Applicant | SMITH & NEPHEW RICHARDS, INC. 2925 APPLING RD. Bartlett, TN 38133 |
| Contact | Alicia E Farage |
| Correspondent | Alicia E Farage SMITH & NEPHEW RICHARDS, INC. 2925 APPLING RD. Bartlett, TN 38133 |
| Product Code | ETB |
| CFR Regulation Number | 874.3450 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-02-28 |
| Decision Date | 1995-03-15 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00821925030626 | K950887 | 000 |