The FDA issued the warning letter on June 21, 2010 as a result of deficiencies in Alphatec Spine’s letter regarding an FDA inspection that occurred in Feb. 2010. A follow-up audit of the company’s facility resulted in an FDA issued close-out letter dated Sept. 28, 2011, that stated the company has resolved issues stated in the letter of warning.
Related Articles on Orthopedic Device Companies:
Orthofix Promotes Bryan McMillan to President of Spine Global Business Unit
K2M Announces Two New Cervical Spine Devices
Zimmer Sponsors 2011 Zimmer Winter National Senior Games
