Precision Spine® Announces 510(k) Clearance of the ShurFit® ACIF 2C System
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| Title: | Precision Spine® Announces 510(k) Clearance of the ShurFit® ACIF 2C System |
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| Authors: | Precision Spine, Inc. |
| Source: | Business Wire (English). 01/18/2017. |
| Abstract: | Precision Spine, Inc., a medical device company dedicated to Made-in-the-USA manufacturing, has announced today that it recently received 510(k) clearance of its ShurFit® ACIF 2C Anterior Cervical Interbody System, which is made from medical grade polyetheretherketone (Peek Optima, LT1) and coated with both commercially pure Titanium (Ti) and Hydroxyapatite (HA). The innovative combination of two proven biomaterials is expected to provide a superior solution to physicians working to achieve biologic fusion. [ABSTRACT FROM PUBLISHER] |
| Database: | Regional Business News |
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| Abstract: | Precision Spine, Inc., a medical device company dedicated to Made-in-the-USA manufacturing, has announced today that it recently received 510(k) clearance of its ShurFit® ACIF 2C Anterior Cervical Interbody System, which is made from medical grade polyetheretherketone (Peek Optima, LT1) and coated with both commercially pure Titanium (Ti) and Hydroxyapatite (HA). The innovative combination of two proven biomaterials is expected to provide a superior solution to physicians working to achieve biologic fusion. [ABSTRACT FROM PUBLISHER] |
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