The following data is part of a premarket notification filed by Treace Medical, Inc. with the FDA for Partial Ossicular Replacement.
| Device ID | K823917 |
| 510k Number | K823917 |
| Device Name: | PARTIAL OSSICULAR REPLACEMENT |
| Classification | Replacement, Ossicular Prosthesis, Total |
| Applicant | TREACE MEDICAL, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | ETA |
| CFR Regulation Number | 874.3495 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-12-28 |
| Decision Date | 1983-06-24 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00681490035729 | K823917 | 000 |
| 00763000035457 | K823917 | 000 |