Bionx Implants, Inc.
Bionx Implants, Inc. holds FDA 510(k) medical device clearances, first cleared 1998, most recent 2002.
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.