Howmedica Osteonics Corp., Dba Stryker Orthopaedics
FDA 510(k) medical device clearances.
Name variants for Howmedica Osteonics Corp., Dba Stryker Orthopaedics
as filed with FDA- Howmedica Osteonics Corp., Dba Stryker Orthopaedics
- Howmedica Osteonics Corp (Dba Stryker Orthopaedics)
Top product codes for Howmedica Osteonics Corp., Dba Stryker Orthopaedics
Recent clearances by Howmedica Osteonics Corp., Dba Stryker Orthopaedics
- K261624 — Omnifit® 20° Series I Insert;Omnifit® Crossfire® 10° Series II Insert; Constrained Acetabular Insert; Trident® Crossfire® 0° Polyethylene Insert; Trident ® Crossfire ® 10° Polyethylene Insert;System 12 Crossfire® 10° Insert; Trident® 0° Constrained Acetabular Insert; Trident® Constrained Acetabular Liner;Trident® All Poly Constrained Acetabular Insert; Crossfire® Eccentric Insert 10°; Artisan® Bone Plug;UHR® Universal Head Bipolar Component
- K253637 — Triathlon® Total Knee System - Triathlon® X3® Medial Stabilized Tibial Bearing Insert
- K252898 — Triathlon® Tritanium® Asymmetric Patella; Triathlon® Tritanium® Symmetric Patella; Triathlon® Symmetric Patella; Triathlon® Asymmetric Patella; Scorpio® Universal Dome Patella; Triathlon® Hinge Bumper
- K252044 — Triathlon® Total Knee System - Triathlon® Gold Femoral Components
- K250989 — Stryker and Serf hip devices
- K251665 — Triathlon® Hinge Knee System
- K243784 — Stryker Orthopaedics Hip Devices Labeling Update
- K243817 — Scorpio Universal Dome Patella; Scorpio Total Stabilizer Insert; Scorpio-Flex Posterior Stabilized Tibial Insert; Scorpio-Flex Cruciate Retaining Tibial Insert; Scorpio NRG Tibial Bearing Insert Cruciate Retaining Insert; Scorpio NRG Tibial Bearing Insert Posteriorly Stabilized Insert
- K242831 — Triathlon Knee System; Triathlon Pro Posterior Stabilized Femoral Components; Triathlon Tritanium Tibial Baseplate; Triathlon Low Profile Tibial Tray; Triathlon Metal Backed Patella; Triathlon Partial Knee System; Avon Patello-femoral Joint Prosthesis; Restoris Multi-Compartmental Knee System
- K241716 — Global Modular Replacement System, Modular Replacement System, Modular Rotating Hinge Knee Component
- K234025 — 22.2mm BIOLOX® delta Ceramic V40 Femoral Heads
- K240418 — Stryker Orthopaedics Hip Systems Labeling Update
- K233724 — 28mm/38D MDM X3 Insert for MDM Liner
- K233498 — Stryker Orthopaedics Hip Systems Labeling Update
- K230952 — Triathlon® Total Knee System - Triathlon® Pro Posterior Stabilized (PS) Femoral Component
- K223069 — Modular Rotating Hinge Knee Systems and Compatible Components
- K222056 — Global Modular Replacement System, Modular Replacement System, Modular Rotating Hinge Knee
- K223528 — Triathlon® Hinge Knee System
- K222632 — UHR Bipolar Implants, Restoration GAP II Implants
- K220376 — Acetabular Dome Hole Plug
- K212187 — Restoration® Modular Hip System
- K213701 — Exeter® X3® RimFit® Cup
- K213129 — Restoration Modular 115mm Conical Distal Stem
- K211303 — Avon Patello-femoral Joint Prosthesis
- K202016 — Dall-Miles® Cable System
- K201343 — Triathlon Total KneeSystem
- K122308 — AXSOS DISTAL LATERAL FEMUR TS LONG PLATES
- K113760 — VARIAX SUPERIOR AND ANTERIOR, LATERAL AND MIDSHAFT CLAVICLE PLATES VARIAX AIMING BLOCKS & JOYSTICK
- K112455 — AIMING BLOCKS FOR VARIAX DISTAL RADIUS PLATES
- K110176 — AXSOS LOCKED PLATING 4.0MM LOCKING INSERTS
- K102282 — THE VARIA FIBULA LOCKED PLATING SYSTEM LINE EXTENSION ADDITION OF STRAIGHT PLATES
- K103010 — STRYKER PATIENT SPECIFIC POLYMER IMPLANT
Data sourced from openFDA. This site is unofficial and independent of the FDA.