Bionx Implants, Inc.
FDA 510(k) medical device clearances.
Top product codes for Bionx Implants, Inc.
Recent clearances by Bionx Implants, Inc.
- K023022 — NUGEN FX SCREW
- K011569 — BIOSORBFX O/M 2.0/2/4 SYSTEM
- K013546 — MODIFICATION TO: 1.5 BONE FIXATION KIT, MODELS BXS6114, BXS6214
- K013057 — BIOCUFF,C, MODELS 236018, 236028, 236036
- K012334 — CONTOUR MENISCUS ARROW, MODELS 541110, 541113, AND 541116
- K010983 — PLLA PIN
- K010554 — MENISCUS ARROW SHEATH #CN1000A; SMARTSCREW ACL SHEATH #SSA2000A
- K010687 — BIOSORBFX AND BIOSORBPDX MESH
- K003659 — PLGA PIN, MODEL 171120,171140,171520,171540,171560,172020,172040,172060,173240,173260
- K003970 — CONTOUR LABRAL NAIL, MODEL 533520A
- K003756 — BIOSORBFX TACK AND BIOSORBPDX TACK BIOABSORBABLE FIXATION FASTENER, USED WITH PLATES
- K001378 — BIOCUFF, MODELS 225718, 225728, 225736, 235718, 235728, 235736
- K000836 — BIOSORBPDX BIOABSORBABLE FIXATION SYSTEM
- K982721 — BIOSORBFX 2.0/2.4 ORTHOGNATHIC AND MANDIBULAR FIXATION SYSTEM
- K982139 — BIOSORBFX 1.5/2.0 BIOABSORBABLE FIXATION SYSTEM
- K972783 — BIOFIX BIODEGRADABLE THREADED SUTURE ANCHOR
- K972919 — BIOFIX BIOABSORBABLE SELF-REINFORCED POLY-L-LACTIDE THREADED BROWLIFT SCREW
- K974876 — BIONX DISTAL RADIUS SCREW
Data sourced from openFDA. This site is unofficial and independent of the FDA.