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510(k) K120590

DILATOR TUBE SET by Koros USA, Inc. — Product Code PDQ

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 7, 2013
Date Received
February 28, 2012
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Neurosurgical Nerve Locator
Device Class
Class II
Regulation Number
874.1820
Review Panel
NE
Submission Type

To locate or monitor function of spinal nerve roots or peripheral nerves during neurosurgery.

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