Theken Spine, LLC
FDA 510(k) & PMA Approved Devices — 23 products
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Total Devices23
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K121482 | INSTRUMENT SYSTEM FOR ENDOSCOPIC SPINAL SURGERY | HRX | 2012-08-28 | View |
| 510(k) | K121211 | VU APOD INTERVERTEBRAL BODY FUSION DEVICE | OVD | 2012-06-27 | View |
| 510(k) | K120829 | STAINLESS STEEL SPINAL SYSTEM | NKB | 2012-05-30 | View |
| 510(k) | K120047 | CORAL SPINAL SYSTEM | NKB | 2012-02-03 | View |
| 510(k) | K111675 | VU C*POD INTERVERTEBRAL BODY FUSION DEVICE | ODP | 2011-08-02 | View |
| 510(k) | K103228 | PARAMOUNT R IBF DEVICE | MAX | 2011-01-05 | View |
| 510(k) | K102323 | CERVICAL STANDALONE INTERVERTEBRAL BODY FUSION DEVICE | OVE | 2010-12-16 | View |
| 510(k) | K101310 | VU APOD INTERVERTEBRAL BODY FUSION DEVICE | OVD | 2010-09-02 | View |
| 510(k) | K100970 | STAINLESS STEEL SPINAL SYSTEM | NKB | 2010-08-12 | View |
| 510(k) | K091266 | THEKEN CORAL SPINAL SYSTEM | NKB | 2009-06-10 | View |
| 510(k) | K083863 | THEKEN ATOLL OCT SPINAL SYSTEM | MNI | 2009-03-27 | View |
| 510(k) | K083073 | THEKEN ATOLL CERVICO-THORACIC SYSTEM | MNI | 2009-03-13 | View |
| 510(k) | K082712 | THEKEN SPINE VU EPOD AND VU LPOD SYSTEM | MAX | 2009-01-02 | View |
| 510(k) | K080822 | VU APOD INTERVERTABRAL BODY FUSION DEVICE | OVD | 2008-07-02 | View |
| 510(k) | K081414 | MODIFICATION TO CORAL SPINAL SYSTEM | NKB | 2008-06-17 | View |
| 510(k) | K080790 | MODIFICATION TO THEKEN ATOLL CERVICO-THORACIC SYSTEM | KWP | 2008-04-29 | View |
| 510(k) | K080690 | MANTA RAY ANTERIOR CERVICAL PLATE SYSTEM | KWQ | 2008-04-25 | View |
| 510(k) | K072407 | BODYFORM THORACIC FIXATION SYSTEM | KWQ | 2007-12-21 | View |
| 510(k) | K070962 | CORAL PEDICLE SCREW SYSTEM | NKB | 2007-08-22 | View |
| 510(k) | K071031 | VU E*POD VERTEBRAL BODY REPLACEMENT | MQP | 2007-07-30 | View |
No matching devices.
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