Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K013671
Device Classification Name
Suture, Absorbable, Synthetic, Polyglycolic Acid
More FDA Info for this Device
510(K) Number
K013671
Device Name
Suture, Absorbable, Synthetic, Polyglycolic Acid
Applicant
UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC
150 GLOVER AVE.
NORWALK, CT 06856 US
Other 510(k) Applications for this Company
Contact
ROBERT ZOTT
Other 510(k) Applications for this Contact
Regulation Number
878.4493
More FDA Info for this Regulation Number
Classification Product Code
GAM
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
11/06/2001
Decision Date
01/08/2002
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
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact