The following data is part of a premarket notification filed by Nobelpharma Usa, Inc. with the FDA for Nobelpharma Bone Anchored Hearing Aid.
| Device ID | K955713 |
| 510k Number | K955713 |
| Device Name: | NOBELPHARMA BONE ANCHORED HEARING AID |
| Classification | Hearing Aid, Bone Conduction |
| Applicant | NOBELPHARMA USA, INC. 777 OAKMONT LN. SUITE 100 Westmont, IL 60559 |
| Contact | Mary Edwards |
| Correspondent | Mary Edwards NOBELPHARMA USA, INC. 777 OAKMONT LN. SUITE 100 Westmont, IL 60559 |
| Product Code | LXB |
| CFR Regulation Number | 874.3300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-12-18 |
| Decision Date | 1996-08-09 |
| Summary: | summary |