Vertebron, Inc.
Vertebron, Inc. holds FDA 510(k) medical device clearances, first cleared 2004, most recent 2008.
Top product codes for Vertebron, Inc.
Recent clearances by Vertebron, Inc.
- K081567 — VERTEBRON SSP CERVICAL PLATING SYSTEM
- K081597 — MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEM
- K073502 — VERTEBRON VBR SYSTEM
- K071376 — MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEM
- K062110 — VERTEBRON SCP CERVICAL PLATE SYSTEM
- K051815 — MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM
- K051716 — VERTEBRON PSS PEDICLE SCREW SYSTEM
- K043152 — VERTEBRON PSS PEDICLE SCREW SYSTEM
- K043181 — MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM
- K040003 — VERTEBRON SCP CERVICAL PLATE SYSTEM
- K033352 — VERTEBRON PSS PEDICLE SCREW SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.