The following data is part of a premarket notification filed by Instratek, Inc. with the FDA for Mini Cannulated Headed And Headless Screw Set.
Device ID | K120493 |
510k Number | K120493 |
Device Name: | MINI CANNULATED HEADED AND HEADLESS SCREW SET |
Classification | Screw, Fixation, Bone |
Applicant | INSTRATEK, INC. 15200 Middlebrook Dr Ste G Houston, TX 77058 |
Contact | Jeff Seavey |
Correspondent | Jeff Seavey INSTRATEK, INC. 15200 Middlebrook Dr Ste G Houston, TX 77058 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-02-17 |
Decision Date | 2012-05-17 |
Summary: | summary |