The following data is part of a premarket notification filed by Smith & Nephew Richards, Inc. with the FDA for Hapex Malleable Torp.
| Device ID | K950927 |
| 510k Number | K950927 |
| Device Name: | HAPEX MALLEABLE TORP |
| Classification | Replacement, Ossicular Prosthesis, Total |
| Applicant | SMITH & NEPHEW RICHARDS, INC. 2925 APPLING RD. Bartlett, TN 38133 |
| Contact | Deborah A Arthur |
| Correspondent | Deborah A Arthur SMITH & NEPHEW RICHARDS, INC. 2925 APPLING RD. Bartlett, TN 38133 |
| Product Code | ETA |
| CFR Regulation Number | 874.3495 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-03-01 |
| Decision Date | 1995-03-21 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00821925030732 | K950927 | 000 |
| 00821925030572 | K950927 | 000 |
| 00821925023567 | K950927 | 000 |
| 00821925023543 | K950927 | 000 |
| 00821925023345 | K950927 | 000 |