510(k) K802838

STERNUM SAW BLADE by Amsco Co. — Product Code GFA

K802838 is an FDA 510(k) premarket notification submitted by Amsco Co. for the device "STERNUM SAW BLADE". The FDA issued a decision of Substantially Equivalent on December 11, 1980. The device falls under product code GFA (Blade, Saw, General & Plastic Surgery, Surgical), a Class I device regulated under 21 CFR 878.4820. Amsco Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 11, 1980
Date Received
November 12, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Blade, Saw, General & Plastic Surgery, Surgical
Device Class
Class I
Regulation Number
878.4820
Review Panel
SU
Submission Type