Medical Device Manufacturer · US , Greenwood , SC

Osteo AG - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1991

Total

Cleared

Denied

Osteo AG has 9 FDA 510(k) cleared medical devices. Based in Greenwood, US.

Historical record: 9 cleared submissions from 1991 to 1994. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Osteo AG Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Osteo AG

9 devices

1-9 of 9

Cleared Jun 30, 1994

OSTEO INTERLOCKING-COMPRESSION NAIL

OSTEO COMPRESSION HIP SCREW

OSTEO COMPLETE PNEUMATIC DRILL-OSCILAIR

K913559 · HSZ

Orthopedic · 90d

Osteo AG - FDA 510(k) Cleared Devices

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