Theken Spine, LLC
Theken Spine, LLC holds FDA 510(k) medical device clearances, first cleared 2007, most recent 2012.
Top product codes for Theken Spine, LLC
Recent clearances by Theken Spine, LLC
- K121482 — INSTRUMENT SYSTEM FOR ENDOSCOPIC SPINAL SURGERY
- K121211 — VU APOD INTERVERTEBRAL BODY FUSION DEVICE
- K120829 — STAINLESS STEEL SPINAL SYSTEM
- K120047 — CORAL SPINAL SYSTEM
- K111675 — VU C*POD INTERVERTEBRAL BODY FUSION DEVICE
- K103228 — PARAMOUNT R IBF DEVICE
- K102323 — CERVICAL STANDALONE INTERVERTEBRAL BODY FUSION DEVICE
- K101310 — VU APOD INTERVERTEBRAL BODY FUSION DEVICE
- K100970 — STAINLESS STEEL SPINAL SYSTEM
- K091266 — THEKEN CORAL SPINAL SYSTEM
- K083863 — THEKEN ATOLL OCT SPINAL SYSTEM
- K083073 — THEKEN ATOLL CERVICO-THORACIC SYSTEM
- K082712 — THEKEN SPINE VU EPOD AND VU LPOD SYSTEM
- K080822 — VU APOD INTERVERTABRAL BODY FUSION DEVICE
- K081414 — MODIFICATION TO CORAL SPINAL SYSTEM
- K080790 — MODIFICATION TO THEKEN ATOLL CERVICO-THORACIC SYSTEM
- K080690 — MANTA RAY ANTERIOR CERVICAL PLATE SYSTEM
- K072407 — BODYFORM THORACIC FIXATION SYSTEM
- K070962 — CORAL PEDICLE SCREW SYSTEM
- K071031 — VU E*POD VERTEBRAL BODY REPLACEMENT
- K070786 — X-POD ADJUSTABLE VERTEBRAL BODY REPLACEMENT
- K070638 — THEKEN ATOLL CERVICO-THORACIC SYSTEM
- K070381 — THEKEN VU MESH VBR SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.