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FDA 510(k) Application Details - K002172
Device Classification Name
Suture, Nonabsorbable, Synthetic, Polyethylene
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510(K) Number
K002172
Device Name
Suture, Nonabsorbable, Synthetic, Polyethylene
Applicant
XIROS PLC
28-30 BLENHEIM TERRACE
LEEDS LS2 9HD GB
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Contact
JIM ROWLAND
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Regulation Number
878.5000
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Classification Product Code
GAT
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More FDA Info for this Product Code
Date Received
07/19/2000
Decision Date
08/28/2001
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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