The following data is part of a premarket notification filed by Spine Wave, Inc. with the FDA for Staxx Fx System.
| Device ID | K053336 |
| 510k Number | K053336 |
| Device Name: | STAXX FX SYSTEM |
| Classification | Cement, Bone, Vertebroplasty |
| 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 | NDN |
| CFR Regulation Number | 888.3027 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-12-01 |
| Decision Date | 2006-07-03 |
| Summary: | summary |