510(k) K102916

G-CATH TISSUE ANCHOR DELIVERY CATHETER by Usgi Medical — Product Code GAT

K102916 is an FDA 510(k) premarket notification submitted by Usgi Medical for the device "G-CATH TISSUE ANCHOR DELIVERY CATHETER". The FDA issued a decision of Substantially Equivalent on October 20, 2010. The device falls under product code GAT (Suture, Nonabsorbable, Synthetic, Polyethylene), a Class II device regulated under 21 CFR 878.5000. Usgi Medical has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 20, 2010
Date Received
October 1, 2010
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Suture, Nonabsorbable, Synthetic, Polyethylene
Device Class
Class II
Regulation Number
878.5000
Review Panel
SU
Submission Type