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FDA 510(k) Applications Submitted by STRAUMANN MANUFACTURING, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K080239
01/31/2008
P.004 ABUTMENTS, P.004 TEMPORARY COPINGS, P.004 PROTECTIVE CAPS, P.004 PERMANENT COPINGS
STRAUMANN MANUFACTURING, INC.
K090260
02/03/2009
MODIFICATION TO:STRAUMANN GUIDED INSTRUMENTS
STRAUMANN MANUFACTURING, INC.
K070478
02/20/2007
P.004 RC TEMPORARY ABUTMENT, P.004 TEMPORARY HEALING ABUTMENT (CAP)
STRAUMANN MANUFACTURING, INC.
K092814
09/14/2009
STRAUMANN DENTAL ABUTMENTS
STRAUMANN MANUFACTURING, INC.
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