Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K024090
Device Classification Name
Suture, Nonabsorbable, Synthetic, Polyamide
More FDA Info for this Device
510(K) Number
K024090
Device Name
Suture, Nonabsorbable, Synthetic, Polyamide
Applicant
AUROLAB
6441 ENTERPRISE LN.
SUITE 214
MADISON, WI 53719 US
Other 510(k) Applications for this Company
Contact
MICHAEL G PRICE
Other 510(k) Applications for this Contact
Regulation Number
878.5020
More FDA Info for this Regulation Number
Classification Product Code
GAR
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
12/11/2002
Decision Date
02/28/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact