Medical Device Manufacturer · US , Malver , PA

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

23 submissions · 23 cleared · Since 2001

Recent clearances: Vitoss Bioactive (BA) Injectable, HydroSet XT, Vitoss BiModal Bone Graft Substitute Foam Strip

23

Total

23

Cleared

0

Denied

FDA 510(k) Regulatory Record - Orthovita, Inc. General Hospital ✕

4 devices

1-4 of 4

Cleared Oct 19, 2005

VITAGEL SURGICAL HEMOSTAT SPRAY SET

General Hospital · 70d

Cleared Apr 16, 2003

IMBIBE II SYRINGE

General Hospital · 85d

Cleared Mar 11, 2003

IMBIBE BONE MARROW ASPIRATION SYRINGE

General Hospital · 176d

Cleared Sep 19, 2001

ORTHOVITA PISTON SYRINGE OR IMBIBE BONE MARROW ASPIRATION SYRINGE

General Hospital · 162d