Stryker Corp.
Stryker Corp. holds FDA 510(k) medical device clearances, first cleared 1976, most recent 2023.
Clearances by Stryker Corp. — page 2
101–124 of 124- K873466 — EXCEL PULSED IRRIGATION/SUCTION SYSTEM
- K871816 — STRYKERSCOPE TM/ORTHOSCOPE TM/STRYKER MINISCOPE TM
- K870745 — STRYKER MODEL 977 BIRTHING BED
- K863447 — STRYKER ORTHOPOWER 90 & ORTHOPOWER 90 SYSTEM II
- K861742 — ELECTRO-SURGICAL PENCILS
- K854077 — MIX EVAC II
- K852674 — STRYKER 988 ICU BED
- K843942 — HENNING MENISCAL SUTURE KIT
- K844214 — COMPARTMENT SYNDROME PRESSURE MONITOR SYS
- K843348 — NISONSON WIRE & DRILL GUIDE SYS
- K834513 — FIXATION STAPLES
- K834515 — FIXATION STAPLE KIT - DLIDE HAMMER
- K834514 — FASCIA CUTTER
- K833509 — CHEMONUCLEOLYSIS TABLE
- K831910 — STRYKER LEG EXERCISER
- K823284 — STRYKER CONSTAVAC
- K811861 — ARTHROSCOPIC LEG HOLDER
- K791349 — SYSTEC 280 INTEGRATED SUCTION SYSTEM
- K771418 — PIN RETRACTORS
- K771199 — SURGIPULSE HEART RATE MONITOR
- K771200 — ORTHOSCOPE
- K770118 — CARPENTER BONE CLAMP
- K760456 — TABLE, HAND SURGI
- K760617 — MIX EVAC BONE CEMENT
Data sourced from openFDA. This site is unofficial and independent of the FDA.