510(k) K821024

DISP. SKIN STAPLER REMOVALBLE SKINSTAPLE by Howmedica Corp. — Product Code GDT

K821024 is an FDA 510(k) premarket notification submitted by Howmedica Corp. for the device "DISP. SKIN STAPLER REMOVALBLE SKINSTAPLE". The FDA issued a decision of Substantially Equivalent on May 14, 1982. The device falls under product code GDT (Staple, Removable (Skin)), a Class I device regulated under 21 CFR 878.4760. Howmedica Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 14, 1982
Date Received
April 13, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Staple, Removable (Skin)
Device Class
Class I
Regulation Number
878.4760
Review Panel
SU
Submission Type