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 |