Pain Concepts, Inc.
DEKOMPRESSOR PERCUTANEOUS LUMBAR DISCECTOMY PROBE
SKU K013513UPC HRX
In Stock
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IIFDA 510(k) Cleared (K013513)
1
Free shipping on orders over $99 · 30-day returns
Pain Concepts, Inc.
Free shipping on orders over $99 · 30-day returns
DEKOMPRESSOR PERCUTANEOUS LUMBAR DISCECTOMY PROBE is an FDA 510(k)-cleared medical device (K013513) manufactured by Pain Concepts, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 16, 2002. Regulation: 8.
