Smith & Nephew Endoscopy, Inc.
FDA 510(k) & PMA Approved Devices — 18 products
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Total Devices18
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K103309 | OSTEORAPTOR CURVED 2.3 SUTURE ANCHORS | MAI | 2011-02-03 | View |
| 510(k) | K102660 | BIORAPTOR CURVED 2.3 PK SUTURE ANCHORS | MBI | 2010-12-13 | View |
| 510(k) | K093428 | SMITH & NEPHEW KNOTLESS INSTABILITY ANCHOR | MBI | 2009-12-17 | View |
| 510(k) | K083226 | SMITH & NEPHEW PEEK INTERFERENCE SCREW | MBI | 2009-01-30 | View |
| 510(k) | K083635 | SMITH & NEPHEW BIOSURE PK INTERFERENCE SCREW | MBI | 2009-01-30 | View |
| 510(k) | K082095 | ULTRASLIDE ACROMIOCLAVICULAR AND SYNDESMOTIC REPAIR DEVICE | HTN | 2008-10-21 | View |
| 510(k) | K050580 | SMITH & NEPHEW INTELIJET FLUID MANAGEMENT SYSTEMS | HRX | 2005-04-20 | View |
| 510(k) | K992396 | BIORCI SCREW | HWC | 2000-01-12 | View |
| 510(k) | K991500 | SMITH & NEPHEW SUTURE LOK | OCW | 1999-07-14 | View |
| 510(k) | K972599 | ACUFEX SCREW CANNULA | HWC | 1997-09-19 | View |
| 510(k) | K971939 | SMITH & NEPHEW SUTURE COLLET | OCW | 1997-08-06 | View |
| 510(k) | K970949 | SMITH & NEPHEW MIS INSTRUMENTS | GCJ | 1997-04-23 | View |
| 510(k) | K970416 | ACUFEX DOUBLE ARMED SUTURE NEEDLE | GAT | 1997-04-21 | View |
| 510(k) | K964935 | SUTURE LOCK | KGS | 1997-02-25 | View |
| 510(k) | K964215 | ACUFEX MOSAICPLASTY COMPREHENSIVE SYSTEM | HRX | 1996-12-20 | View |
| 510(k) | K963901 | ELECTROSURGICAL PROBE | GEI | 1996-11-04 | View |
| 510(k) | K962789 | SURGICAL KIT-ACUFEX MOSAICPLASTY SYSTEM | GEY | 1996-08-14 | View |
| 510(k) | K961649 | ACUFEX TIBIAL ANCHOR SCREW & SPIKED WASHER | HWC | 1996-07-16 | View |
No matching devices.
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