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 |