OSSIOfiber® Suture Anchor System - Two 4.75 mm with Tape, #2 Sutures, with Need
OSSIOfiber® Suture Anchor System - Two 4.75 mm with Tape, #2 Sutures, with Needles. Package contains: 1 OSSIOfiber Suture Anchor, 4.75 mm, Black Tape & Blue/White #2 Sutures with Needles; 1 OSSIOfiber Suture Anchor, 4.75 mm, Black/White Tape & Blue #2 Sutures with Needles; 1 OSSIO Drill Bit & Drill Guide.
OSSIOfiber® Suture Anchor System - Two 4.75 mm with Suture Snare. Package contai
OSSIOfiber® Suture Anchor System - Two 4.75 mm with Suture Snare. Package contains: 2 OSSIOfiber Suture Anchor with Snare, 4.75 mm, 1 OSSIO Punch, 1 Solid Black 2mm Tape Suture, 1 Blue/Black 2mm Tape Suture.
The OSSIOfiber® Hammertoe Fixation Implant, M, 2.9X19 mm, angled 10°. Package c
The OSSIOfiber® Hammertoe Fixation Implant, M, 2.9X19 mm, angled 10°. Package contains: 1 Inserter, 1 Implant angled 10°.
The OSSIOfiber™ Hammertoe Fixation Implant is indicated for maintenance of alig
The OSSIOfiber™ Hammertoe Fixation Implant is indicated for maintenance of alignment and fixation of bone fractures, osteotomies, arthrodesis, and bone grafts in the presence of appropriate additional immobilization (e.g. rigid fixation implants, cast, brace).
The OSSIOfiber® Hammertoe Fixation System, M, 2.9X19 mm, angled 10°. Package co
The OSSIOfiber® Hammertoe Fixation System, M, 2.9X19 mm, angled 10°. Package contains: 1 K-wire, 1 Drill Bit, 1 Inserter, 1 Implant angled 10°.
The OSSIOfiber® Hammertoe Fixation System, M, 2.9X19 mm, straight 0°. Package c
The OSSIOfiber® Hammertoe Fixation System, M, 2.9X19 mm, straight 0°. Package contains: 1 K-wire, 1 Drill Bit, 1 Inserter, 1 Implant straight 0°.
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.