Conmed Linvatec
Largo, FL, US
Conmed Linvatec appears in FDA device records in Largo, FL. FDA records list 21 510(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
- 21
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 21 510(k) clearances for Conmed Linvatec between 2005 and 2011. The busiest year on record is 2007, with 5. The most recent is 2011, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2005 | 1 |
| 2006 | 4 |
| 2007 | 5 |
| 2008 | 4 |
| 2009 | 3 |
| 2010 | 3 |
| 2011 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K111779 | Y-KNOT ALL-SUTURE ANCHOR MODEL HF13 | MBI | Substantially Equivalent | |
| K102410 | MATRYX INTERFERENCE SCREW (5.0-6.5MM) | HWC | Substantially Equivalent | |
| K102339 | CONMED LINVATEC SEQUENT MENISCAL REPAIR DEVICE | GAT | Substantially Equivalent | |
| K101100 | CROSSFT OC SUTURE ANCHOR MODE CFC-4502, CFC-5502, CFC-6502, CFC-4503, CFC-5503, CFC-6503 | MAI | Substantially Equivalent | |
| K092898 | CONMED LINVATEC PRESTO PRELOADED WITH ONE OR TWO #2 HI-FI SUTURES | MAI | Substantially Equivalent | |
| K090560 | CONMED LINVATEC ANODIZED ALUMINUM STERILIZATION TRAYS | KCT | Substantially Equivalent | |
| K083161 | ZEN WIRELESS FOOTSWITCH (W1000), ZEN WIRELESS FOOTSWITCH ADAPTER (W1100) | HRX | Substantially Equivalent | |
| K080531 | CONMED LINVATEC MICROFRACTURE INSTRUMENT STERILIZATION TRAY | KCT | Substantially Equivalent | |
| K072291 | CONMED LINVATEC BIO MINI-REVO SUTURE ANCHOR | HWC | Substantially Equivalent | |
| K080444 | CONMED LINVATEC OSPREY DRILL SYSTEM | HBC | Substantially Equivalent | |
| K073481 | THREVO ANCHOR, DISPOSABLE DRIVER, HI-FI SUTURES | MBI | Substantially Equivalent | |
| K072706 | MICROCHOICE DRILLS AND SAWS, MICROPOWER DRILLS AND SAWS, MICROPOWER ORALMAX HIGH SPEED DRILL | HRX | Substantially Equivalent | |
| K070780 | CONMED LINVATEC XO BUTTON | MBI | Substantially Equivalent | |
| K070376 | CONMED LINVATEC 300W XENON LIGHT SOURCE | GCT | Substantially Equivalent | |
| K070233 | CONMED LINVATEC SMART GUARD IRRIGATOR | HRX | Substantially Equivalent | |
| K063326 | CONMED LINVATEC 24K IRRIGATION SYSTEM | HRX | Substantially Equivalent | |
| K063457 | TRUEHD (1080P) DIGITAL CAMERA SYSTEM | GCJ | Substantially Equivalent | |
| K052992 | CONMED LINVATEC INSTRUMENT STERILIZATION TRAY | FRG | Substantially Equivalent | |
| K060714 | HI-FI ULTRAFIX KNOTLESS MINIMITE SUTURE ANCHOR | HWC | Substantially Equivalent | |
| K053561 | BIO-MINI REVO SUTURE ANCHOR | HWC | Substantially Equivalent | |
| K050923 | LIGHTWAVE INTEGRATED ELECTRODE ABLATOR AND LIGHT WAVE INTEGRATED ELECTRODE SUCTION ABLATOR | JOS | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- HRXArthroscope
- JOSElectrode, Electrosurgical
- MAIFastener, Fixation, Biodegradable, Soft Tissue
- MBIFastener, Fixation, Nondegradable, Soft Tissue
- GCJLaparoscope, General & Plastic Surgery
- GCTLight Source, Endoscope, Xenon Arc
- HBCMotor, Drill, Electric
- HWCScrew, Fixation, Bone
- KCTSterilization Wrap Containers, Trays, Cassettes & Other Accessories
- GATSuture, Nonabsorbable, Synthetic, Polyethylene
- FRGWrap, Sterilization
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