Medical Device Manufacturer · NL , Bilthoven

Isotis Orthobiologics, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 2004

Total

Cleared

Denied

Isotis Orthobiologics, Inc. has 10 FDA 510(k) cleared orthopedic devices. Based in Bilthoven, NL.

Historical record: 10 cleared submissions from 2004 to 2009.

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 - Isotis Orthobiologics, Inc.

10 devices

1-10 of 10

ORTHOBLAST II DBM DEMINERALIZED BONE MATRIX PASTE AND PUTTY

K070751 · MQV

Orthopedic · 210d

Cleared Dec 05, 2005

ORTHOBLAST II PUTTY AND PASTE

K050642 · MBP

Orthopedic · 269d

Cleared Sep 07, 2005

CONNEXUS, .5CC, MODEL 023000-005

ASPIREX - BONE MARROW ASPIRATE KIT

K041991 · FMF

General Hospital · 55d

Isotis Orthobiologics, Inc. - FDA 510(k) Cleared Devices

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