Northern Digital, Inc.
Northern Digital, Inc. holds FDA 510(k) medical device clearance, cleared in 2004, with 2 FDA device recalls on record.
Top product codes for Northern Digital, Inc.
FDA recalls by Northern Digital, Inc.
- Z-2084-2015 — NDI Disposable Reflective Marker Spheres for Brainlab IGS (Image Guided Surgical) system. Product Usage: Disposable reflective marker spheres are attached to reference arrays and instruments, thus enabling the infrared tracking systems to detect the position of the patient and instruments in the surgical field.
- Z-2093-2015 — NDI Disposable Reflective Marker Spheres for Brainlab IGS (Image Guided Surgery) system. Product Usage: Disposable reflective marker spheres are attached to reference arrays and instruments, thus enabling the infrared tracking systems to detect the position of the patient and instruments in the surgical field.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Northern Digital, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.