Acromed Corp.
FDA 510(k) & PMA Approved Devices — 41 products
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Total Devices41
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K980485 | ISOLA SPINAL SYSTEM | MNI | 1998-10-21 | View |
| 510(k) | K981714 | TIMX LOW BACK SYSTEM TITANIUM MX ROD BASED LOW BACK SYSTEM | MNH | 1998-06-30 | View |
| 510(k) | K981113 | PEDIATRIC PRC | MNH | 1998-05-29 | View |
| 510(k) | K981274 | ACROMED TIMX PLATE BASED LOW BACK SYSTEM | MNH | 1998-04-29 | View |
| 510(k) | K980228 | UNIVERSITY PLATE ANTERIOR SYSTEM | KWQ | 1998-04-14 | View |
| 510(k) | K974757 | KANEDA ANTERIOR SCOLIOSIS SYSTEM KASS | KWQ | 1998-03-05 | View |
| 510(k) | K972718 | M-2 ANTERIOR PLATE SYSTEM | KWQ | 1997-10-01 | View |
| 510(k) | K971248 | KANEDA SR ANTERIOR SPINAL SYSTEM | KWQ | 1997-06-11 | View |
| 510(k) | K970955 | ACROMED ANTERIOR CERVICAL STABILIZATION SYSTEM | KWQ | 1997-06-11 | View |
| 510(k) | K970950 | EASY ROD | MNH | 1997-06-03 | View |
| 510(k) | K965102 | ACROMED PEDICLE SCREW | MNH | 1997-05-08 | View |
| 510(k) | K970462 | ACROMED ANTERIOR CERVICAL STABILIZATION SYSTEM | KWQ | 1997-04-03 | View |
| 510(k) | K965046 | ISOLA TWISTER CONNECTOR | MNH | 1997-03-14 | View |
| 510(k) | K953978 | ANTERIOR DYNAMIZED SYSTEM | KWQ | 1997-02-19 | View |
| 510(k) | K964007 | ACROMED CABLE/WIRE PEDICLE SCREW | MNH | 1996-12-16 | View |
| 510(k) | K962984 | ISOLA PEDIATRIC COMPONENTS | KWP | 1996-11-27 | View |
| 510(k) | K963639 | ACROMED PEDICLE SCREW | KWP | 1996-11-14 | View |
| 510(k) | K962645 | ISOLA TWISTER CONNECTOR | MNH | 1996-10-22 | View |
| 510(k) | K952236 | ISOLA SYSTEM | MNH | 1996-01-22 | View |
| 510(k) | K951657 | VSP (VARIABLE SCREW PLACEMENT) SPINAL FIXATION SYSTEM, PEDICLE SCREW(S), SPINE PLATE(S), WASHER(S) & NUT(S) | MNH | 1995-08-21 | View |
No matching devices.
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