The following data is part of a premarket notification filed by Avanta Orthopaedics, Inc. with the FDA for Scaphix, Staple, Fixation, Bone.
| Device ID | K003033 |
| 510k Number | K003033 |
| Device Name: | SCAPHIX, STAPLE, FIXATION, BONE |
| Classification | Staple, Fixation, Bone |
| 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 | JDR |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-09-28 |
| Decision Date | 2001-05-30 |