510(k) K802524

Device: Surgical Hammers
Applicant: MIDSHORE WELDING CORP.
510(k) number: K802524
Product code: FZY
Decision: Substantially Equivalent (SESE)
Decision date: 1980-11-12
Date received: 1980-10-16
Regulation: 878.4800
Classification name: Hammer, Surgical
Medical specialty: General, Plastic Surgery
Review panel: General, Plastic Surgery
Device class: 1
Clearance type: Traditional
Third party reviewed: No

Applicant Contact#

Address: 803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA