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FDA 510(k) Application Details - K990090
Device Classification Name
Suture, Nonabsorbable, Synthetic, Polyamide
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510(K) Number
K990090
Device Name
Suture, Nonabsorbable, Synthetic, Polyamide
Applicant
AESCULAP, INC.
13221 MARICOTTE PLACE
SAN DIEGO, CA 92130 US
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Contact
STEVE REITZLER
Other 510(k) Applications for this Contact
Regulation Number
878.5020
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Classification Product Code
GAR
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More FDA Info for this Product Code
Date Received
01/11/1999
Decision Date
03/22/1999
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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