Medical Device Manufacturer · US , Potomac , MD

New Deal, S.A. - FDA 510(k) Cleared Devices

28 submissions · 28 cleared · Since 1999

Total

Cleared

Denied

New Deal, S.A. has 28 FDA 510(k) cleared orthopedic devices. Based in Potomac, US.

Historical record: 28 cleared submissions from 1999 to 2007.

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 - New Deal, S.A.

28 devices

1-12 of 28

MODIFICATION TO TTC PLATES

K070160 · HRS

Orthopedic · 22d

Cleared Feb 08, 2007

MODIFICATION TO LAPIDUS PLATE

LARGE UNI-CLIP STAPLE

KALIX II IMPLANT, MODEL 141 0XX WITH XX

New Deal, S.A. - FDA 510(k) Cleared Devices

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