Orthovita, Inc.
FDA 510(k) & PMA Approved Devices — 20 products
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Total Devices20
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K163621 | Vitoss Bioactive (BA) Injectable | MQV | 2017-05-02 | View |
| 510(k) | K161447 | HydroSet XT | MQV | 2016-10-06 | View |
| 510(k) | K153608 | Vitoss BiModal Bone Graft Substitute Foam Strip | MQV | 2016-02-12 | View |
| 510(k) | K103173 | VITOSS BA BIMODAL BIOACTIVE BONE GRAFT SUBSTITUTE | MQV | 2011-02-07 | View |
| 510(k) | K101171 | ORTHOVITA PEEK SPACER | ODP | 2011-01-25 | View |
| 510(k) | K102545 | FM-02 BONE GRAFT SUBSTITUTE | MQV | 2010-10-27 | View |
| 510(k) | K091618 | VITOMATRIX | LYC | 2010-09-27 | View |
| 510(k) | K080108 | CORTOSS BONE AUGMENTATION MATERIAL | NDN | 2009-06-05 | View |
| 510(k) | K083033 | VITOSS BONE GRAFT SUBSTITUTE, BONE GRAFT SUBSTITUTE FILLED CANISTER, FOAM & BIOACTIVE FOAM BONE GRAFT SUBSTITUTE | MQV | 2008-11-06 | View |
| 510(k) | K081439 | VITOSS BIOACTIVE FOAM PACK BONE GRAFT SUBSTITUTE | MQV | 2008-06-17 | View |
| 510(k) | K072184 | VITOSS BIOACTIVE FOAM BONE GRAFT SUBSTITUTE | MQV | 2007-09-18 | View |
| 510(k) | K052173 | VITAGEL SURGICAL HEMOSTAT SPRAY SET | FMF | 2005-10-19 | View |
| 510(k) | K050795 | IMBIBE BONE MARROW ASPIRATION NEEDLE | KNW | 2005-06-03 | View |
| 510(k) | K032288 | VITOSS SCAFFOLD FOAM BONE GRAFT MATERIAL | MQV | 2003-12-19 | View |
| 510(k) | K032812 | ENDOSKELETON TA VERTEBRAL BODY REPLACEMENT | MQP | 2003-12-08 | View |
| 510(k) | K032130 | VITOSS-FILLED CARTRIDGE | MQV | 2003-11-05 | View |
| 510(k) | K032409 | VITOSS SCAFFOLD SYNTHETIC CANCELLOUS BONE VOID FILLER | MQV | 2003-08-29 | View |
| 510(k) | K030208 | IMBIBE II SYRINGE | FMF | 2003-04-16 | View |
| 510(k) | K023074 | IMBIBE BONE MARROW ASPIRATION SYRINGE | FMF | 2003-03-11 | View |
| 510(k) | K011087 | ORTHOVITA PISTON SYRINGE OR IMBIBE BONE MARROW ASPIRATION SYRINGE | FMF | 2001-09-19 | View |
No matching devices.
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