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 |