The following data is part of a premarket notification filed by Zavation Medical Products, Llc with the FDA for Si Screw System.
| Device ID | K173752 |
| 510k Number | K173752 |
| Device Name: | SI Screw System |
| Classification | Sacroiliac Joint Fixation |
| Applicant | Zavation Medical Products, LLC 220 Lakeland Parkway Flowood, MS 39232 |
| Contact | James M. Phillips |
| Correspondent | Milton Phillips Zavation Medical Products, LLC 220 Lakeland Parkway Flowood, MS 39232 |
| Product Code | OUR |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-12-08 |
| Decision Date | 2018-03-16 |
| Summary: | summary |