Vertebron, Inc.
Stratford, CT, US
Vertebron, Inc. appears in FDA device records in Stratford, CT. FDA records list 11 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 11
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 11 510(k) clearances for Vertebron, Inc. between 2004 and 2008. The busiest year on record is 2004, with 3. The most recent is 2008, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2004 | 3 |
| 2005 | 3 |
| 2006 | 1 |
| 2007 | 1 |
| 2008 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K081567 | VERTEBRON SSP CERVICAL PLATING SYSTEM | KWQ | Substantially Equivalent | |
| K081597 | MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEM | MNI | Substantially Equivalent | |
| K073502 | VERTEBRON VBR SYSTEM | MQP | Substantially Equivalent | |
| K071376 | MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEM | NKB | Substantially Equivalent | |
| K062110 | VERTEBRON SCP CERVICAL PLATE SYSTEM | KWQ | Substantially Equivalent | |
| K051815 | MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM | KWQ | Substantially Equivalent | |
| K051716 | VERTEBRON PSS PEDICLE SCREW SYSTEM | KWP | Substantially Equivalent | |
| K043152 | VERTEBRON PSS PEDICLE SCREW SYSTEM | MNH | Substantially Equivalent | |
| K043181 | MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM | KWQ | Substantially Equivalent | |
| K040003 | VERTEBRON SCP CERVICAL PLATE SYSTEM | KWQ | Substantially Equivalent | |
| K033352 | VERTEBRON PSS PEDICLE SCREW SYSTEM | MNI | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain