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About This Item
Full Description
1.1 This test method covers poly(L-lactic acid) resin intended for use in surgical implants.
1.2 The requirements of this test method apply to poly(Llactic acid) in various forms:
1.2.1 Virgin polymer, or
1.2.2 Any form fabricated from virgin polymer such as a semi-finished component of a finished product, a finished product, which may include packaged and sterilized implants, or a specially fabricated test specimen.
Document History
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ASTM F1635-16
Standard Test Method for in vitro Degradation Testing of Hydrolytically Degradable Polymer Resins and Fabricated Forms for Surgical Implants- Most Recent
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ASTM F1635-11
Standard Test Method for in vitro Degradation Testing of Hydrolytically Degradable Polymer Resins and Fabricated Forms for Surgical Implants- Historical Version
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ASTM F1635-04a
Standard Test Method for in Vitro Degradation Testing of Hydrolytically Degradable Polymer Resins and Fabricated Forms for Surgical Implants- Historical Version
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ASTM F1635-04
Standard Test Method for in Vitro Degradation Testing of Hydrolytically Degradable Polymer Resins and Fabricated Forms for Surgical Implants- Historical Version
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ASTM F1635-95(2000)
Standard Test Method for In Vitro Degradation Testing of Poly (L-lactic Acid) Resin and Fabricated Form for Surgical Implants- Historical Version
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ASTM F1635-95
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Standard Test Method for In Vitro Degradation Testing of Poly (L-lactic Acid) Resin and Fabricated Form for Surgical Implants- Historical Version