The following data is part of a premarket notification filed by Fusion Orthopedics, Llc with the FDA for Hammertechtm Fixation System.
Device ID | K182684 |
510k Number | K182684 |
Device Name: | HammerTechTM Fixation System |
Classification | Screw, Fixation, Bone |
Applicant | Fusion Orthopedics, LLC 4135 S. Power Rd., Suite 110 Mesa, AZ 85212 |
Contact | Eli Jacobson |
Correspondent | Eli Jacobson Fusion Orthopedics, LLC 4135 S. Power Rd., Suite 110 Mesa, AZ 85212 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-09-26 |
Decision Date | 2018-11-23 |
Summary: | summary |