FDA IDE Approval
-
Recon
Maxx Orthopedics, in Partnership with Invibio Biomaterial Solutions, Secures US IDE Approval for PEEK-OPTIMA™ Total Knee Arthroplasty Study
The PEEK-OPTIMA femoral component is based on Maxx Orthopedics’ Freedom Total Knee System high-flexion, bone-conserving design. The study will compare…
Read More » -
Hospitals
Bio2 Technologies, Inc. Receives FDA IDE Approval to Begin Clinical Study of Resorbable Cervical Interbody Device for Spinal Fusion
WOBURN, Mass., Nov. 13, 2018 /PRNewswire/ — Bio2 Technologies, Inc., a privately held orthopedics company, announced today that it received U.S. Food and…
Read More » -
Hospitals
Cerapedics Receives FDA IDE Approval to Initiate Study of P-15L Bone Graft for Transforaminal Lumbar Interbody Fusion Surgery
WESTMINSTER, Colo., March 14, 2018 /PRNewswire/ — Cerapedics, a privately-held orthobiologics company, today announced the company received approval from the U.S. Food…
Read More »