Interpore Intl.
INTERPORE 200 POROUS HYDROXYAPATITE
SKU K860983UPC LYC
In Stock
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IIFDA 510(k) Cleared (K860983)
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Free shipping on orders over $99 · 30-day returns
Interpore Intl.
Free shipping on orders over $99 · 30-day returns
INTERPORE 200 POROUS HYDROXYAPATITE is an FDA 510(k)-cleared medical device (K860983) manufactured by Interpore Intl.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 22, 1986. Regulation: 8.
