Linvatec Corp.
Linvatec Corp. appears in FDA public data with 0 recalls, 93 510(k) clearances, 6 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 23, 2009.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 93
- Inspections
- 6
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K092998 | CONMED LINVATEC INTERCEPT IMPLANT | December 23, 2009 |
| K091549 | CONMED LINVATEC SOFT TISSUE TO BONE SYSTEM | June 23, 2009 |
| K090835 | CONMED LINVATEC BIO MINI-REVO SUTURE ANCHOR, MODEL C6170CR | June 22, 2009 |
| K090186 | CONMED LINVATEC PALADIN, PRELOADED WITH TWO #2 HI-FI SUTURES | April 10, 2009 |
| K083281 | EL LIGHTWAVE SUCTION ABLATOR, MODEL EL-2000-S, LIGHTWAVE SUCTION ABLATOR, MODEL IA-2000-S, LIGHTWAVE | February 25, 2009 |
| K060198 | MICROPOWER HAND PIECE : MEDIUM SPEED DRILL, SAGGITAL SAW, RECIPROCATING SAW, AND OSCILLATING SAW | May 11, 2006 |
| K060270 | MICROPOWER HAND PIECE: ORAL MAX HIGH SPEED DRILL | April 10, 2006 |
| K060260 | MICROPOWER HAND PIECE HIGH SPEED DRILL | April 10, 2006 |
| K050519 | ADVANCED TURBO DRIVE SYSTEM | May 17, 2005 |
| K050497 | BIOSCREW XTRALOK, 8X35MM & 8X40MM VIOLET | March 25, 2005 |
| K050227 | THREVO SUTURE ANCHOR WITH DISPOSABLE DRIVER | March 2, 2005 |
| K043106 | PINN-ACL CROSSPIN | January 19, 2005 |
| K042778 | BIOANCHOR WITH DISPOSABLE DRIVER, PRELOADED WITH ONE #2 HERCULINE SUTURE | November 4, 2004 |
| K041128 | SUTURE ARROW | July 29, 2004 |
| K041713 | SUPER REVO HERCULINE SUTURE ANCHOR | July 22, 2004 |
| K033573 | LINVATEC 10K IRRIGATION SYSTEM | February 11, 2004 |
| K033804 | BIOANCHOR WITH DISPOSABLE DRIVER | December 31, 2003 |
| K033748 | TRIDENT RESECTION ABLATOR | December 15, 2003 |
| K032607 | POWERPRO PNEUMATIC SYSTEM, MODELS PRO6150, PRO6175, PRO6185 | November 10, 2003 |
| K031994 | LINVATEC 300W XENON LIGHT SOURCE | August 21, 2003 |