
Plexus Intl., Inc.
Free shipping on orders over $99 · 30-day returns
ORTHO-PLEX-REHABILITATION SYSTEM is an FDA 510(k)-cleared medical device (K920686) manufactured by Plexus Intl., Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 10, 1992. Regulation: 8.

Synthes (Usa)
SKU K100676
BackorderedMedline
SKU VM-1270020

Cardinal Health
SKU VM-1270026
BackorderedMoog
SKU VM-1270057