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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K792206
Device Name MEDTRONIC BURR HOLE PLUG & CAP
Applicant
Medtronic Vascular
4221 Richmond Rd., NW
Walker,  MI  49534
Correspondent
Medtronic Vascular
4221 Richmond Rd., NW
Walker,  MI  49534
Date Received10/29/1979
Decision Date 11/21/1979
Decision Substantially Equivalent (SESE)
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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