The following data is part of a premarket notification filed by Zimmer Spine, Inc with the FDA for Dynesys Top-loading Spinal System.
| Device ID | K092234 |
| 510k Number | K092234 |
| Device Name: | DYNESYS TOP-LOADING SPINAL SYSTEM |
| Classification | Posterior Metal/polymer Spinal System, Fusion |
| Applicant | ZIMMER SPINE, INC 7375 BUSH LAKE RD. Minneapolis, MN 55439 -2027 |
| Contact | Elsa A Linke |
| Correspondent | Elsa A Linke ZIMMER SPINE, INC 7375 BUSH LAKE RD. Minneapolis, MN 55439 -2027 |
| Product Code | NQP |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-07-23 |
| Decision Date | 2009-10-01 |
| Summary: | summary |