Memometal Technologies
Bruz, FR
Memometal Technologies appears in FDA device records in Bruz, FR. FDA records list 10 510(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
- 10
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 10 510(k) clearances for Memometal Technologies between 2007 and 2011. The busiest year on record is 2007, with 5. The most recent is 2011, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2007 | 5 |
| 2009 | 1 |
| 2010 | 2 |
| 2011 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K112197 | MEMOMETAL INTRA-MEDULLARY BONE FASTENER | HTY | Substantially Equivalent | |
| K101930 | MEMOMETAL NAVIS BONE PLATING SYSTEM | HRS | Substantially Equivalent | |
| K102072 | MEMOMETAL IMPLANTS (K-SNAP & TI-FUSE) | HTY | Substantially Equivalent | |
| K093820 | SUBFIX ARTHROEREISIS IMPLANT, MODELS SUT0065, SUT0080, SUT0090, SUT0100, SUT0115 | HWC | Substantially Equivalent | |
| K083447 | MEMOMETAL ANCHORAGE BONE PLATE SYSTEM, MODELS PLSS/PLSL, PLP10/PLP20/PLP30/PLP40/PLP50 | HRS | Substantially Equivalent | |
| K071941 | MEMOMETAL BONE ANCHORS | HWC | Substantially Equivalent | |
| K070598 | MEMOMETAL INTRA-MEDULLARY BONE FASTENER, MODELS SMART TOE / X-FUSE | HTY | Substantially Equivalent | |
| K070039 | MEMOMETAL FIXOS SCREWS | HWC | Substantially Equivalent | |
| K070033 | MEMOMETAL VARISATION, MODELS AV26-08, AV26-10, AV90-08 AND AV90-10 | JDR | Substantially Equivalent | |
| K070031 | MEMOMETAL MEMORY STAPLES | JDR | 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