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510(k) K041201

ULTRACLIP II MR by Inrad — Product Code GDW

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 3, 2004
Date Received
May 7, 2004
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Staple, Implantable
Device Class
Class II
Regulation Number
878.4750
Review Panel
SU
Submission Type

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