Intermedics Orthopedics
Intermedics Orthopedics holds FDA 510(k) medical device clearances, first cleared 1982, most recent 1997.
Clearances by Intermedics Orthopedics — page 2
101–108 of 108- K822320 — KAMPNER FEMORAL COMPONENT
- K821341 — IOI METAL BACKED TIBIAL COMPONENT
- K821343 — BDH FEMORAL COMPONENT
- K821340 — VARIAXIAL CONSTRAINED TOTAL KNEE PROSTH.
- K821342 — METAL BACKED ACETABULAR COMPONENT
- K813598 — 101 TOTAL CONDYLAR KNEE SYSTEM
- K813599 — 101-32 FEMORAL COMPONENT
- K813600 — AUFRANC-TURNER TYPE ACETABULAR COMPON
Data sourced from openFDA. This site is unofficial and independent of the FDA.