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FDA 510(k) Application Details - K030351
Device Classification Name
Suture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile
More FDA Info for this Device
510(K) Number
K030351
Device Name
Suture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile
Applicant
CP MEDICAL
836 N.E. 24TH AVE.
PORTLAND, OR 97232 US
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Contact
MARY ANN GREENAWALT
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Regulation Number
878.4495
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Classification Product Code
GAQ
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More FDA Info for this Product Code
Date Received
02/03/2003
Decision Date
03/28/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Abbreviated
Reviewed By Third Party
N
Expedited Review
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