Bionx Implants, Ltd.
FDA 510(k) & PMA Approved Devices — 12 products
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Total Devices12
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K030388 | IMPACT SUTURE ANCHOR. MODEL 433510 | HWC | 2003-04-24 | View |
| 510(k) | K020056 | DUET SUTURE ANCHOR | HWC | 2002-06-26 | View |
| 510(k) | K012000 | 1.5MM BONE FIXATION KIT | HWC | 2001-07-18 | View |
| 510(k) | K012001 | SMARTSCREW | HWC | 2001-07-18 | View |
| 510(k) | K003077 | SMARTSCREW MODEL 222006...227510 | HWC | 2001-04-26 | View |
| 510(k) | K003757 | THERMOFX MESH | JEY | 2001-02-07 | View |
| 510(k) | K000616 | SMARTWEDGE ACL, MODELS 430623, 430628, 430723, 430728, 430823, 430828 | MAI | 2000-03-23 | View |
| 510(k) | K993074 | SMART NAIL MODELS 521516, 521520,521525, 531516, 531520. 531525 | MAI | 1999-12-10 | View |
| 510(k) | K993073 | SMART SCREW ACL MODELS 237020, 237025, 237030, 238020, 238025, 238030, 239020, 239025, 239030 | MAI | 1999-12-06 | View |
| 510(k) | K993453 | MENISCUS ARROW, MODELS 531110, 531113, 531116 | MAI | 1999-11-09 | View |
| 510(k) | K992947 | CANNULATED SMARTSCREW MODELS 224540C, 224570C | HWC | 1999-09-21 | View |
| 510(k) | K992567 | ANATOMICAL BANKART TACK, MODEL 523520A | MAI | 1999-08-27 | View |
No matching devices.
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