Precision Spine Receives FDA Clearance for Mini-Max Spine System

Precision Spine received FDA 510(k) clearance for its Mini-Max Minimally Invasive Access System.

Advertisement

The expansion of Precision Spine’s minimally invasive spine solutions will give surgeons the ability to perform access and fixation procedures as precisely as their open counterparts.

Mini-Max is intended for use with Precision’s S-LOK Pedicle Screw System for immobilization and stabilization of spinal segments as an adjunct to fusion.

More Articles on Devices:
Biovenus Opens Dutch Headquarters
Sens. Amy Klobuchar, Al Franken Seek to Delay Medical Device Tax
36 Orthopedic & Spine Devices Receive FDA 510(k) Clearance in November

At the Becker’s 32nd Annual Meeting: The Business and Operations of ASCs, taking place October 29-31 in Chicago, ASC leaders, surgeons and healthcare executives will explore strategies to drive growth, enhance operational performance, navigate reimbursement challenges and prepare for the future of ambulatory surgery. Apply for complimentary registration now.

Watch On-Demand Webinar

ASC development + private equity: How to build value from day one

Presenters: Andrew HrankaWendy Bruno Thomson, MBA, LHARichard Romero, CVA, ABV, FHFMA, PAHM

Advertisement

Next Up in Spinal Tech

Advertisement

Comments are closed.