From Privi Medical’s FDA clearance to OrthoXel getting FDA clearance and CE Mark approval, here are seven medtech stories we missed this week but thought were still worth mentioning. 1. Privi Medical wins FDA nod for hemorrhoid device Privi Medical has received FDA clearance for its Instalief Hemorrhoids Treatment device, according to a Jan. 18 news […]
FDA clears Centric Medical’s hammertoe device
Centric Medical, the foot & ankle division of Life Spine, said today it won FDA 510(k) clearance for its Hammertoe Correction System. The newly cleared system is designed to be inserted between the proximal and middle phalanges so opposing threads fixate on the phalangeal canal of the to to compress the joint, the Huntley, Ill.-based company said. “Due […]
Life Spine’s foot & ankle division, Centric Medical, wins FDA nod for flatfoot implant
Centric Medical, the foot & ankle division of Life Spine, said yesterday that it won 510(k) clearance from the FDA for its subtalar arthroereisis implant for treating flatfoot deformities. The device is a 1-piece titanium implant designed to block forward, downward and medial displacement of the talus to allow normal articulation of the subtalar joint. The device is slated for limited release at […]
BSX wins CE Mark, FDA approval for spinal cord stims | Regulatory news for the week of October 27, 2014
Boston Scientific wins CE Mark, FDA nod for spinal surgical leads
October 21, 2014 by Brad Perriello
Life Spine creates Centric Medical ankle & foot unit
Life Spine launched a new division called Centric Medical, after receiving FDA marketing clearance for its Tarsa-Link system for internal bone fixation of fractures, fusions, and osteotomies in the foot and ankle.
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