Vertebral Technologies, Inc.
FDA 510(k) medical device clearances.
Top product codes for Vertebral Technologies, Inc.
Recent clearances by Vertebral Technologies, Inc.
- K131540 — INTERFUSE L INTERVERTEBRAL BODY FUSION DEVICE
- K110226 — INTERFUSE T INVERTEBRAL BODY FUSION DEVICE
- K110045 — INTERFUSE DA INVERTEBRAL BODY FUSION DEVICE
- K102277 — INTERFUSE T INVERTEBRAL BODY FUSION DEVICE
- K093675 — INTERFUSE INVERTEBRAL BODY FUSION DEVICE MODEL 9076
- K091988 — MODIFICATION TO: INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE , MODEL 9076
- K080673 — INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE
Data sourced from openFDA. This site is unofficial and independent of the FDA.