The following data is part of a premarket notification filed by Spinecraft, Inc. with the FDA for Apex Spine System 5.50 Mm Titanium Rod & Polyaxial Screw Washer.
Device ID | K092825 |
510k Number | K092825 |
Device Name: | APEX SPINE SYSTEM 5.50 MM TITANIUM ROD & POLYAXIAL SCREW WASHER |
Classification | Appliance, Fixation, Spinal Interlaminal |
Applicant | SPINECRAFT, INC. 2215 ENTREPRISE DR. Westchester, IL 60154 -5804 |
Contact | Ami Akallal-asaad |
Correspondent | Ami Akallal-asaad SPINECRAFT, INC. 2215 ENTREPRISE DR. Westchester, IL 60154 -5804 |
Product Code | KWP |
Subsequent Product Code | MNH |
Subsequent Product Code | MNI |
CFR Regulation Number | 888.3050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-09-11 |
Decision Date | 2010-03-16 |
Summary: | summary |