Hohenstein Enterprises, Inc.
FDA 510(k) & PMA Approved Devices — 1 products
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Total Devices1
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K022665 | POROUS HDPE SURGICAL IMPLANTS, TO BE DISTRIBUTED UNDER VARIOUS TRADEMARKS INCLUDING EPOR, BIOPOR, MINOPOR & P-HDPE | KKY | 2002-10-09 | View |
No matching devices.
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