The following data is part of a premarket notification filed by Alphatec/nexmed with the FDA for Novel Vbr Spinal System.
| Device ID | K042201 |
| 510k Number | K042201 |
| Device Name: | NOVEL VBR SPINAL SYSTEM |
| Classification | Spinal Vertebral Body Replacement Device |
| Applicant | ALPHATEC/NEXMED 6110 CORTE DEL CEDRO Carlsbad, CA 92009 |
| Contact | Ellen Yarnall |
| Correspondent | Ellen Yarnall ALPHATEC/NEXMED 6110 CORTE DEL CEDRO Carlsbad, CA 92009 |
| Product Code | MQP |
| CFR Regulation Number | 888.3060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-08-13 |
| Decision Date | 2004-10-07 |
| Summary: | summary |