Alphatec Mfg., Inc.
Alphatec Mfg., Inc. holds FDA 510(k) medical device clearances, first cleared 1990, most recent 2004.
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.