The following data is part of a premarket notification filed by Seaspine, Inc. with the FDA for Seaspine Vbr System.
Device ID | K052170 |
510k Number | K052170 |
Device Name: | SEASPINE VBR SYSTEM |
Classification | Spinal Vertebral Body Replacement Device |
Applicant | SEASPINE, INC. 2303 LA MIRADA DR. Vista, CA 92081 -7862 |
Contact | Diana Smith |
Correspondent | Diana Smith SEASPINE, INC. 2303 LA MIRADA DR. Vista, CA 92081 -7862 |
Product Code | MQP |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-08-09 |
Decision Date | 2005-12-21 |
Summary: | summary |