Integrated Surgical Systems, Inc.
ORTHODOC PREOPERATIVE PLANNER MODEL 500
SKU K960685UPC HWT
In Stock
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IFDA 510(k) Cleared (K960685)
1
Free shipping on orders over $99 · 30-day returns
Integrated Surgical Systems, Inc.
Free shipping on orders over $99 · 30-day returns
ORTHODOC PREOPERATIVE PLANNER MODEL 500 is an FDA 510(k)-cleared medical device (K960685) manufactured by Integrated Surgical Systems, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 16, 1997. Regulation: 8.
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