510(k) K050947

MODIFICATION TO: MODIFIED USS POLYPROPYLENE SUTURE by United States Surgical, A Division of Tyco Healthc — Product Code GAW

K050947 is an FDA 510(k) premarket notification submitted by United States Surgical, A Division of Tyco Healthc for the device "MODIFICATION TO: MODIFIED USS POLYPROPYLENE SUTURE". The FDA issued a decision of Substantially Equivalent on June 1, 2005. The device falls under product code GAW (Suture, Nonabsorbable, Synthetic, Polypropylene), a Class II device regulated under 21 CFR 878.5010. United States Surgical, A Division of Tyco Healthc has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 1, 2005
Date Received
April 15, 2005
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Suture, Nonabsorbable, Synthetic, Polypropylene
Device Class
Class II
Regulation Number
878.5010
Review Panel
SU
Submission Type