The following data is part of a premarket notification filed by Spine Wave, Inc. with the FDA for Staxx Xd System.
| Device ID | K052670 |
| 510k Number | K052670 |
| Device Name: | STAXX XD SYSTEM |
| Classification | Spinal Vertebral Body Replacement Device |
| Applicant | SPINE WAVE, INC. TWO ENTERPRISE DR. SUITE 302 Shelton, CT 06484 |
| Contact | Ronald K Smith |
| Correspondent | Ronald K Smith SPINE WAVE, INC. TWO ENTERPRISE DR. SUITE 302 Shelton, CT 06484 |
| Product Code | MQP |
| CFR Regulation Number | 888.3060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-09-27 |
| Decision Date | 2006-04-27 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10840642100600 | K052670 | 000 |
| 10840642100594 | K052670 | 000 |