Spine Smith Partners L.P.
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K122630 | IN:C2 SPINAL FIXATION SYSTEM | OVE | 2012-12-05 | View |
| 510(k) | K122168 | VISUALIF CHALLENGING ACCESS PLATE | OVD | 2012-10-11 | View |
| 510(k) | K102090 | SPINESMITH CYNCH SPINAL SYSTEM - VISUALIF INTERBODY FUSION IMPLANT SYSTEM | OVD | 2010-09-30 | View |
| 510(k) | K101085 | SPINESMITH CYNCH SPINAL SYSTEM | MAX | 2010-07-01 | View |
| 510(k) | K090376 | SPINESMITH CYNCH SPINAL SYSTEM | MAX | 2009-04-01 | View |
| 510(k) | K082821 | SPINESMITH PARTNERS, LP CEQUENCE ANTERIOR CERVICAL PLATE SYSTEM | KWQ | 2008-10-31 | View |
| 510(k) | K081132 | SPINESMITH PARTNERS, LP CEQUENCE ANTERIOR CERVICAL PLATE SYSTEM | KWQ | 2008-07-14 | View |
| 510(k) | K080971 | SPINESMITH CIMPLICITY SPINAL SYSTEM | MQP | 2008-07-02 | View |
| 510(k) | K073320 | CIMPLICITY SPINAL SYSTEM | ODP | 2008-02-07 | View |
No matching devices.
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