Fusion Orthopedics is pleased to introduce the LSI Arthroereisis Peg System as the newest addition to their product offering. The LSI Peg Implant is an updated iteration of the highly reputable implant created by Dr. Sgarlato, a renowned surgeon and pioneer in foot and ankle surgical and biomechanical methods. The...
HammerTech Titanium Straight and Angled Inventory is Now Available
Fusion Orthopedics is pleased to announce that HammerTech Titanium inventory is now in-stock and available for national distribution. The new Class II titanium devices are a welcomed addition to the PEEK implants in the existing HammerTech implant family and are indicated for fixation and osteotomies of the lesser toes following...
Fusion Orthopedics Receives 510K Clearance on new Small Bone Plating System
Fusion Orthopedics is pleased to introduce the PolyLock Plating System as the newest addition to their product offering. FDA 510(k) clearance was issued November 18th, 2019. The assigned FDA 510(k) # for the Plating System is K192323. The PolyLock System is indicated for use in the treatment of bone fractures,...
Fusion Orthopedics Receives 510K FDA Clearance on new Silastic System
Fusion Orthopedics Receives 510K FDA Approval on new Silastic System Fusion Orthopedics is pleased to announce an expanded and new Silastic System as the newest addition to their product offering. FDA 510(k) clearance was issued October 21st, 2019. The assigned FDA 510(k) # for Silastic System is K190136. The new...
Fusion Orthopedics Receives HammerTech Titanium 510K FDA Approval
Fusion Orthopedics Receives HammerTech Titanium 510K FDA Approval Fusion Orthopedics is pleased to announce HammerTech Titanium as the newest addition to their product offering. FDA 510(k) clearance was issued November 23rd, 2018. The assigned FDA 510(k) # for HammerTech is K182684. The new Class II titanium devices are a welcomed...
DynaBridge Staple System – FDA Cleared
After years of development, Fusion Orthopedics is pleased to announce the DynaBridge System as the newest addition to their product offering. FDA 510(k) clearance was issued October 15th, 2018. The assigned FDA 510(k) # for DynaBridge is K181815. The system is indicated for fracture and osteotomy fixation and joint arthrodesis...
TalarLift STS – FDA Cleared
We are pleased to announce the TalarLift STS as the newest addition to the Fusion Orthopedics product offering. FDA 510(k) clearance was issued August 11th, 2017. The assigned FDA 510(k) # for TalarLift STS is K170624. The TalarLift STS is a comprehensive arthroereisis system indicated for use in the treatment...
FuzeFix Screw System – FDA Cleared
We are pleased to announce the FuzeFix Screw system as the newest addition to the FDA cleared Fusion Orthopedics product offering. FDA 510(k) approval was issued August 7, 2017. The assigned FDA 510(k) # for the FuzeFix Screw System is K170038. The FuzeFix Screw System consists of: Headed Compression Screws from...