The following data is part of a premarket notification filed by Acromed Corp. with the FDA for Casf (tm) (contoured Anterior Spinal Fixaton Sys.).
| Device ID | K904446 |
| 510k Number | K904446 |
| Device Name: | CASF (TM) (CONTOURED ANTERIOR SPINAL FIXATON SYS.) |
| Classification | Appliance, Fixation, Spinal Intervertebral Body |
| Applicant | ACROMED CORP. 3303 CARNEGIE AVE. Cleveland, OH 44115 |
| Contact | William Christianson |
| Correspondent | William Christianson ACROMED CORP. 3303 CARNEGIE AVE. Cleveland, OH 44115 |
| Product Code | KWQ |
| CFR Regulation Number | 888.3060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-09-28 |
| Decision Date | 1991-09-05 |