Alphatec Mfg., Inc.
FDA 510(k) medical device clearances.
Top product codes for Alphatec Mfg., Inc.
Recent clearances by Alphatec Mfg., Inc.
- K033090 — ICON POLYAXIAL PEDICLE SCREW SYSTEM
- K023299 — ALPHA MIRAGE TOP TIGHTENING SPINAL SYSTEM
- K020356 — ALPHA MIRAGE TOP TIGHTENING SPINAL SYSTEM
- K993513 — DELTALOC ANTERIOR CERVICAL PLATE SYSTEM
- K993873 — ALPHATEC EXTERNAL FIXATION SYSTEM COMPRESSION/DISTRACTION ROD
- K992350 — PYLON INTRAMEDULLAARY NAIL SYSTEM
- K980788 — ALPHATEC WIRE EXTERNAL FIXATION SYSTEM
- K964400 — ALPHATEC EXTERNAL FIXATION SYSTEM
- K951846 — MIRAGE SPINAL SYSTEM FOR SEVERE SPONDYLOLISTHESIS
- K926417 — ALPHATEC 130-150 SLOTTED COMPRESSION HIP SCREW
- K930515 — ALPHA SPINAL SYSTEM
- K933112 — ALPHATEC COMPRESSION AND RECONSTRUCTION PLATES
- K925500 — ALPHATEC 130 COMPRESSION HIP SCREW
- K923256 — ALPHATEC 2.7 MM CANNULATED CORTICAL LAG SCREW
- K922166 — ALPHATEC SMALL FRAGMENT SET
- K922167 — ALPHATEC COMPRESSION AND RECONSTRUCTION PLATES
- K922322 — ALPHATEC 3.5MM ZNNULATED CORTICAL LAG SCREW
- K921622 — ALPHATEC COMPRESSION HIP SCREW SYSTEM
- K914004 — ALPHATEC CANNULATED BONE SCREWS
- K894959 — CYPRESS CERVICAL TRACTION EQUIPMENT, CYPRESS HALO
Data sourced from openFDA. This site is unofficial and independent of the FDA.