Recognition List Number: 026 Publication Date: 03/18/2011
Part B: SUPPLEMENTARY INFORMATION
Recognition Number 3-87: ASTM F 2477-07, Standard Test Methods for in vitro Pulsatile Durability. (Cardiovascular)
Date of Standard: 2007. |
| Address of Standards Organization: |
| ASTM International (ASTM) |
| 100 Barr Harbor Drive |
| West Conshohocken, PA 19428-2959 |
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| CDRH Office and Division Associated with Recognized Standards: |
| OFFICE OF DEVICE EVALUATION (ODE) | | DIVISION OF CARDIOVASCULAR DEVICES (DCD) |
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| Devices Affected: |
| Vascular stents (including coronary and peripheral, and bare metal and drug-eluting stents) |
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| Processes Affected: |
| PMA, IDE, PDP, HDE, Design Control Input, Quality System Regulation |
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| Extent of Recognition: |
Complete standard
NOTE: This standard identifies critical parameters for endovascular systems and provides guidance on the development of appropriate test methods. It does not contain acceptance criteria for the parameters. |
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| Related CFR Citations and Product Codes: |
Regulation
Number |
Device Name |
Device
Class |
Product
Code |
| Unclassified |
Coronary Drug-Eluting Stent |
Class 3 |
NIQ |
| Unclassified |
Stent, Carotid |
Class 3 |
NIM |
| Unclassified |
Stent, Coronary |
Class 3 |
MAF |
| Unclassified |
Stent, Iliac |
Class 3 |
NIO |
| Unclassified |
Stent, Renal |
Class 3 |
NIN |
| Unclassified |
Stent, Superficial Femoral Artery |
Class 3 |
NIP |
| |
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| Relevant Guidance: |
| Guidance for Industry and FDA Staff - Non-Clinical Engineering Tests and Recommended Labeling for Intravascular Stents and Associated Delivery Systems |
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| FDA Technical Contact: |
| Kenneth Cavanaugh |
| FDA/CDRH/ODE |
| 10903 New Hampshire Avenue Building 66, Room 1208 |
| Silver Spring MD 20993 |
| 301/796-6377 |
| Email: kenneth.cavanaugh@fda.hhs.gov |
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