The following data is part of a premarket notification filed by Avanta Orthopaedics, Inc. with the FDA for Ulnar Head Implant.
| Device ID | K982268 |
| 510k Number | K982268 |
| Device Name: | ULNAR HEAD IMPLANT |
| Classification | Prosthesis, Wrist, Hemi-, Ulnar |
| Applicant | AVANTA ORTHOPAEDICS, INC. 9369 CARROLL PARK DRIVE, STE.A San Diego, CA 92121 |
| Contact | Louise M Focht |
| Correspondent | Louise M Focht AVANTA ORTHOPAEDICS, INC. 9369 CARROLL PARK DRIVE, STE.A San Diego, CA 92121 |
| Product Code | KXE |
| CFR Regulation Number | 888.3810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-06-29 |
| Decision Date | 1998-12-04 |
| Summary: | summary |