Medical Device Manufacturer · US , San Mateo , CA

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

24 submissions · 21 cleared · Since 1985

Total

Cleared

Denied

Osteotech, Inc. has 21 FDA 510(k) cleared orthopedic devices. Based in San Mateo, US.

Historical record: 21 cleared submissions from 1985 to 2008.

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 - Osteotech, Inc.

24 devices

1-12 of 24

Cleared Oct 16, 2008

GRAFTON R II EDBM, DEMINERALIZED BONE MATRIX ALLOGRAFT, RESORBABLE CALCIUM...

GRAFTON PLUS DBM PASTE

K042707 · NUN

Dental · 426d

Cleared Nov 23, 2005

GRAFTON PLUS DBM PASTE

K043048 · MBP

Orthopedic · 384d

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

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