• FDA 510(k) records for SONICAID SYSTEM 8002 K992607
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FDA 510(k) K062842, TWIST DRILL, by Walter Lorenz Surgical, Inc.

FDA 510(k) K062842, TWIST DRILL, by Walter Lorenz Surgical, Inc.

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510(K) Number: K062842
Device Name: TWIST DRILL
Manufacturer: Walter Lorenz Surgical, Inc.
Device Classification Name: drills, burrs, trephines & accessories (simple, powered)
Regulation Number: 882.4310
Classification Product Code: HBE
Date Received: 09/22/2006
Decision Date: 12/04/2006
Regulation Medical Specialty: Neurology
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