FDA 510(k) Application Details - K011698

Device Classification Name Plate, Bone

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510(K) Number K011698
Device Name Plate, Bone
Applicant INSTITUT STRAUMANN AG
RESERVOIR PLACE
1601 TRAPELO ROAD
WALTHAM, MA 02451 US
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Contact LINDA JALBERT
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Regulation Number 872.4760

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Classification Product Code JEY
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Date Received 06/01/2001
Decision Date 08/23/2001
Decision SESE - SUBST EQUIV
Classification Advisory Committee DE - Dental
Review Advisory Committee DE - Dental
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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