Medical Device Manufacturer · US , San Mateo , CA

Osteotech, Inc. - FDA 510(k) Cleared Devices

24 submissions · 21 cleared · Since 1985

24

Total

21

Cleared

0

Denied

FDA 510(k) Regulatory Record - Osteotech, Inc. Pathology ✕

1 devices

1-1 of 1

Cleared Oct 13, 1988

ALLOPREP SYSTEM

Pathology · 85d