Product received FDA 510(k) clearance for: small bone fixation, reconstruction a
Product received FDA 510(k) clearance for: small bone fixation, reconstruction and fusion such as inter-digital fusion of fingers and toes. Pre-sterilized, all inclusive implant procedure tray contains: 1ea Instrument containing a Nitinol IFS implant held in instrument with a locking pin; 3ea K-wires with sharps protection, and 1ea Drill Bit with integral handle for manual use.
Product received FDA 510(k) clearance for: small bone fixation, reconstruction a
Product received FDA 510(k) clearance for: small bone fixation, reconstruction and fusion such as inter-digital fusion of fingers and toes. Pre-sterilized, all inclusive implant procedure tray contains; 1ea Instrument containing a Nitinol IFS implant held in instrument with a locking pin; 1ea 1.1mm (0.045") double trocar k-wire with sharps protection, and 1ea 2.7mm Drill Bit with integral handle for manual use.
'Product received FDA 510(k) clearance for: small bone fixation, reconstruction
'Product received FDA 510(k) clearance for: small bone fixation, reconstruction and fusion such as inter-digital fusion of fingers and toes. Pre-sterilized, all inclusive implant procedure tray contains: 1ea Instrument containing a Nitinol IFS implant held in place with a locking pin; 1ea 1.1mm (0.045") Double trocar K-wire with sharps protection, and 1ea 2.7mm Drill Bit with handle for manual use.
Product received FDA 510(k) clearance for: small bone fixation, reconstruction a
Product received FDA 510(k) clearance for: small bone fixation, reconstruction and fusion such as inter-digital fusion of fingers and toes. Pre-sterilized, all inclusive implant procedure tray contains; 1ea Instrument containing a Nitinol IFS implant held in instrument with a locking pin; 1ea 1.1mm (0.045") double trocar k-wire with sharps protection, and 1ea 2.7mm Drill Bit with integral handle for manual use.
Product received FDA 510(k) clearance for: small bone fixation, reconstruction a
Product received FDA 510(k) clearance for: small bone fixation, reconstruction and fusion such as inter-digital fusion of fingers and toes. Pre-sterilized, all inclusive implant procedure tray contains: 1ea Instrument containing a Nitinol IFS implant held in instrument with a locking pin; 1ea 1.1mm (0.045") Double trocar K-wire with sharps protection, and 1ea 2.7mm Drill Bit with integral handle for manual use.
Product received FDA 510(k) clearance for: small bone fixation, reconstruction a
Product received FDA 510(k) clearance for: small bone fixation, reconstruction and fusion such as inter-digital fusion of fingers and toes. Pre-sterilized, all inclusive implant procedure tray contains: 1ea Instrument containing a Nitinol IFS implant held in instrument with a locking pin, 1ea 1.1mm (0.045") double trocar K-wire with sharps protection, and 1ea 2.7mm Drill Bit with integral handle for manual use.
Product received FDA 510(k) clearance for: small bone fixation, reconstruction a
Product received FDA 510(k) clearance for: small bone fixation, reconstruction and fusion such as inter-digital fusion of findgers and toes. Pre-sterilized, all inclusive implant procedure tray contains: 1ea Instrument containing a Nitinol Intramedullary Fixation Scaffold (SuperScaffold™) implant held in place by use of a locking pin; 1ea 1.1mm (0.045") double trocar K-wire with sharps protection, and 1ea 2.2mm Drill Bit with integral handle for manual use.