510(k) K020804

AUTO SUTURE PREMIUM PLUS CEEA DISPOSABLE STAPLER by United States Surgical, A Division of Tyco Healthc — Product Code GDW

K020804 is an FDA 510(k) premarket notification submitted by United States Surgical, A Division of Tyco Healthc for the device "AUTO SUTURE PREMIUM PLUS CEEA DISPOSABLE STAPLER". The FDA issued a decision of Substantially Equivalent on November 19, 2002. The device falls under product code GDW (Staple, Implantable), a Class II device regulated under 21 CFR 878.4750. 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
November 19, 2002
Date Received
March 12, 2002
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Staple, Implantable
Device Class
Class II
Regulation Number
878.4750
Review Panel
SU
Submission Type