Medical Device Manufacturer · US , Foster City , CA

J.B.S., S.A. - FDA 510(k) Cleared Devices

10 submissions · 6 cleared · Since 1994

Total

Cleared

Denied

J.B.S., S.A. has 6 FDA 510(k) cleared orthopedic devices. Based in Foster City, US.

Historical record: 6 cleared submissions from 1994 to 1996.

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 - J.B.S., S.A.

10 devices

1-10 of 10

Cleared Sep 25, 1996

J.B.S. SPINE SYSTEM WITH PEDICLE SCREWS - ADDITIONAL COMPONENTS - SCREWS,...

SPINE SYSTEM SACRAL PLATE

SPINAL PEDICLE SCREW, FIXATION, APPLIANCE

K952298 · MNH

Orthopedic · 211d

Cleared Jul 11, 1995

J.B.S. CERVICAL SPINE SYSTEM

K942432 · KWP

Orthopedic · 417d

Cleared Nov 14, 1994

JBS SMOOTH FIXATION PIN

J.B.S. SELF-TAPPING THREADED PIN

K940673 · HTY

Orthopedic · 271d

Cleared Oct 19, 1994

J.B.S. IMPLANTABLE SPINAL FIXATION DEVICE

K935113 · KWP

Orthopedic · 359d

J.B.S., S.A. - FDA 510(k) Cleared Devices

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