The following data is part of a premarket notification filed by Acromed Corp. with the FDA for Acromed Timx Plate Based Low Back System.
| Device ID | K981274 |
| 510k Number | K981274 |
| Device Name: | ACROMED TIMX PLATE BASED LOW BACK SYSTEM |
| Classification | Orthosis, Spondylolisthesis Spinal Fixation |
| Applicant | ACROMED CORP. 3303 CARNEGIE AVE. Cleveland, OH 44115 |
| Contact | Mary Lewis |
| Correspondent | Mary Lewis ACROMED CORP. 3303 CARNEGIE AVE. Cleveland, OH 44115 |
| Product Code | MNH |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-04-08 |
| Decision Date | 1998-04-29 |
| Summary: | summary |