The following data is part of a premarket notification filed by Tyber Medical Llc with the FDA for Tyber Medical Trauma Screw.
Device ID | K153575 |
510k Number | K153575 |
Device Name: | Tyber Medical Trauma Screw |
Classification | Screw, Fixation, Bone |
Applicant | TYBER MEDICAL LLC 89 HEADQUARTERS PLAZA NORTH #1464 Morristown, NJ 07960 |
Contact | Mark F Schenk |
Correspondent | Mark F Schenk TYBER MEDICAL LLC 89 HEADQUARTERS PLAZA NORTH #1464 Morristown, NJ 07960 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-12-15 |
Decision Date | 2016-02-26 |
Summary: | summary |