Trans1 Incorporated
FDA 510(k) medical device clearances.
Top product codes for Trans1 Incorporated
Recent clearances by Trans1 Incorporated
- K120991 — TRANS1 INTERBODY FUSION SYSTEM
- K102334 — TRANS1 AXIALIF PLUS
- K100210 — TRANS1 LATERAL INTERVERTEBRAL FUSION DEVICE, T
- K092124 — AXIALIF 2L, AXIALIF 2-LEVEL SYSTEM, AXIALIF APOLLO, AXIALIF II
- K073643 — TRANS1 AXIALIF 2-LEVEL OR II SYSTEM
- K073515 — TRANS1 FACET SCREW
- K073514 — TRANS1 AXIAL FIXATON SYSTEM
- K051856 — TRANS1 FACET SCREWS
- K050965 — TRANS1 AXIALIF SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.