Depuy Ireland UC
FDA 510(k) medical device clearances.
Name variants for Depuy Ireland UC
as filed with FDA- Depuy Ireland UC
- DePuy Ireland UC
Top product codes for Depuy Ireland UC
Recent clearances by Depuy Ireland UC
- K260480 — VELYS Robotic-Assisted Solution
- K261458 — ATTUNE Total Knee System; ATTUNE Cementless Knee System
- K260536 — Prostalac Hip System, SmartSet V+G Dual Antibiotic Bone Cement
- K253624 — INHANCE Reverse Shoulder System
- K253551 — VELYS Hip Navigation
- K253197 — ATTUNE Total Knee System; ATTUNE Revision Sleeve LPS Femoral Adaptors
- K251292 — RECLAIM Monobloc Revision Femoral Stem
- K243977 — EMPHASYS Acetabular System
- K243248 — INHANCE INTACT
- K242871 — ATTUNE Revision Hinge Knee
- K242084 — EMPHASYS Acetabular Shell with RapiTite HA
- K241000 — ATTUNE Revision Knee System; DePuy Knee Prosthesis System Universal Stem Extensions and Universal Femoral Metaphyseal Sleeves; DePuy Sigma PS Femoral Components; DePuy Sigma Cruciate Retaining (C/R) Porocoat Femoral Components; S-ROM NOILES Rotating Hinge Knee System; DePuy P.F.C. SIGMA Total Knee System; DePuy SIGMA Total Knee System;
- K240678 — ATTUNE® Porous Fixed Bearing Tibial Base, Medialized Dome Patella and Medialized Anatomic Patella with AFFIXIUM 3DP Technology
- K240211 — VELYS Robotic-Assisted Solution
- K240639 — PINNACLETM Constrained Acetabular Liners
- K233980 — ATTUNE Total Knee System, ATTUNE Cementless Knee System, LPS Limb Preservation System, Sigma High Performance (HP) Partial Knee System
- K231522 — EMPHASYS Dual Mobility System
- K231873 — DePuy SUMMIT Porocoat Hip Prosthesis MR Conditional, DePuy SUMMIT DuoFix Hip Prosthesis MR Conditional, DePuy SUMMIT Cemented Hip Prosthesis MR Conditional, DePuy SUMMIT FX Cemented Hip Prosthesis MR Conditional, DePuy SUMMIT Basic Press-Fit Hip Prosthesis MR Conditional
- K231526 — CORAIL Cemented Femoral Stem
- K233227 — VELYS Robotic-Assisted Solution
- K232303 — ATTUNE® Porous Fixed Bearing Tibial Base, Medialized Dome Patella and Medialized Anatomic Patella with AFFIXIUM 3DP Technology
- K230831 — INHANCE Shoulder System Convertible Glenoid Inserts, INHANCE Convertible Glenoid
- K233233 — EMPHASYS Femoral Stems
- K232556 — DePuy 3D Additive TriFlange Acetabular Cup and DePuy TriFlange II Acetabular Cup System
- K231516 — INHANCE Shoulder System, Sterile Single Use Instrumentation
- K230295 — ATTUNE® Revision Cones
- K222296 — ARTICUL/EZE Ceramic Heads
- K223211 — INHANCETM Shoulder System Humeral Stems and Stemless
- K221462 — DePuy Reclaim Monobloc Revision Femoral Stem
- K212746 — ATTUNE Revision Cones
- K221636 — EMPHASYS Acetabular System
- K221467 — INHANCETM Reverse Glenoid Peripheral Posts
- K220216 — C-Stem AMT LE Prosthesis
- K212933 — INHANCETM Hybrid Anatomic Glenoid Implant
- K212737 — INHANCE Reverse Shoulder System
- K213781 — ATTUNE® Porous Fixed Bearing Tibial Base with AFFIXIUM 3DP
- K212710 — GLOBAL UNITE Platform Shoulder System
- K211609 — ATTUNE Medial Stabilized (MS) Fixed Bearing (FB) Insert
- K211657 — EMPHASYS Femoral Stems
- K203694 — DELTA XTEND Reverse Shoulder System
- K210581 — Actis DuoFix Hip Prosthesis- Collarless
- K203532 — BI-MENTUM ALTRX® Dual Mobility Liner
- K202769 — VELYS Robotic-Assisted Solution
- K202248 — Attune Revision Sleeve LPS Femoral Adaptors
- K202098 — GLOBAL UNITE Platform Shoulder System
- K202194 — ATTUNE® Porous Fixed Bearing Tibial Base, Medialized Dome Patella, and Medialized Anatomic Patella with AFFIXIUM 3DP Technology
- K200854 — DePuy PINNACLE Dual Mobility Liner
- K193549 — SIGMA High Performance (HP) Partial Knee System
- K193057 — ATTUNE All-Polyethylene Tibia
- K170748 — GLOBAL UNITE Platform Shoulder System
Data sourced from openFDA. This site is unofficial and independent of the FDA.