Arthocare Corporation
Harrogate, North Yorkshire, GB
Arthocare Corporation appears in FDA device records in Harrogate, North Yorkshire, GB. FDA records list 6 510(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
- 6
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 6 510(k) clearances for Arthocare Corporation between 2001 and 2016. The busiest year on record is 2012, with 3. The most recent is 2016, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2001 | 1 |
| 2012 | 3 |
| 2013 | 1 |
| 2016 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K153669 | MultiFIX S Ultra Knotless Fixation System | MBI | Substantially Equivalent | |
| K131182 | MULTIFIX S KNOTLESS FIXATION DEVICE | MBI | Substantially Equivalent | |
| K120791 | AMBIENT TURBOFLASH 90 IFS | GEI | Substantially Equivalent | |
| K123268 | SMARTSTITCH PERFECTPASSER SYSTEM | GAT | Substantially Equivalent | |
| K121306 | SMARTSTITCH M-CONNECTOR ULTRA SMARTSTITCH SUTURE DEVICE HANDLE SMARTSTITCH SUTURE DEVICE HANDLE | GAT | Substantially Equivalent | |
| K013334 | ENDOFLIP | MBI | 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