Medical Device Manufacturer · US , Mchenry , IL

Black & Decker(Tm) - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 1980

Total

Cleared

Denied

Black & Decker(Tm) has 11 FDA 510(k) cleared orthopedic devices. Based in Mchenry, US.

Historical record: 11 cleared submissions from 1980 to 1982.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Black & Decker(Tm)

11 devices

1-11 of 11

Cleared Mar 02, 1982

CAST CUTTER/CAST SAW/INSTRUMENT

General & Plastic Surgery · 68d

Cleared Nov 02, 1981

SAGITTAL SAW

K812438 · GEY

General & Plastic Surgery · 68d

Black & Decker(Tm) - FDA 510(k) Cleared Devices

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