
Interpore Intl.
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INTERPORE IMZ(CASTABLE)TUB/SCRET RET RIGID ATTACH is an FDA 510(k)-cleared medical device (K901928) manufactured by Interpore Intl.. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 25, 1990. Regulation: 8.