The following data is part of a premarket notification filed by Theken Surgical with the FDA for Coral Spinal System.
| Device ID | K041592 |
| 510k Number | K041592 |
| Device Name: | CORAL SPINAL SYSTEM |
| Classification | Appliance, Fixation, Spinal Interlaminal |
| Applicant | THEKEN SURGICAL 283 E. WATERLOO ROAD Akron, OH 44203 |
| Contact | Randy Theken |
| Correspondent | Randy Theken THEKEN SURGICAL 283 E. WATERLOO ROAD Akron, OH 44203 |
| Product Code | KWP |
| Subsequent Product Code | KWQ |
| Subsequent Product Code | MNH |
| Subsequent Product Code | MNI |
| Subsequent Product Code | NKB |
| CFR Regulation Number | 888.3050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-06-14 |
| Decision Date | 2004-09-16 |
| Summary: | summary |