Name: PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER
Brand: Interventional Spine, Inc.
SKU: K090767

PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER is an FDA 510(k)-cleared medical device (K090767) manufactured by Interventional Spine, Inc.. This device is classified under the Unknown specialty. FDA Device Class U. FDA clearance granted on June 10, 2009.

PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER

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