Theken Spine, LLC
FDA 510(k) medical device clearances.
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.