Cerapedics completed a US $22MM financing. Proceeds will support continued launch of i-FACTOR™ Peptide Enhanced Bone Graft and a second Level I investigational device exemption (IDE) human clinical study.
The round was led by KCK Group, a family investment fund.
Cerapedics received FDA Premarket Approval in 2015 for use of i-FACTOR in anterior cervical discectomy and fusion, and was the first PMA-approved bone graft with this indication. The company has also initiated an IDE clinical trial in transforaminal lumbar interbody fusion.
Source: Cerapedics; ORTHOWORLD Inc.
Cerapedics completed a US $22MM financing. Proceeds will support continued launch of i-FACTOR™ Peptide Enhanced Bone Graft and a second Level I investigational device exemption (IDE) human clinical study.
The round was led by KCK Group, a family investment fund.
Cerapedics received FDA Premarket Approval in 2015 for use of i-FACTOR in...
Cerapedics completed a US $22MM financing. Proceeds will support continued launch of i-FACTOR™ Peptide Enhanced Bone Graft and a second Level I investigational device exemption (IDE) human clinical study.
The round was led by KCK Group, a family investment fund.
Cerapedics received FDA Premarket Approval in 2015 for use of i-FACTOR in anterior cervical discectomy and fusion, and was the first PMA-approved bone graft with this indication. The company has also initiated an IDE clinical trial in transforaminal lumbar interbody fusion.
Source: Cerapedics; ORTHOWORLD Inc.
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JV
Julie Vetalice is ORTHOWORLD's Editorial Assistant. She has covered the orthopedic industry for over 20 years, having joined the company in 1999.