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Linvatec Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
93
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K092998CONMED LINVATEC INTERCEPT IMPLANTDecember 23, 2009
K091549CONMED LINVATEC SOFT TISSUE TO BONE SYSTEMJune 23, 2009
K090835CONMED LINVATEC BIO MINI-REVO SUTURE ANCHOR, MODEL C6170CRJune 22, 2009
K090186CONMED LINVATEC PALADIN, PRELOADED WITH TWO #2 HI-FI SUTURESApril 10, 2009
K083281EL LIGHTWAVE SUCTION ABLATOR, MODEL EL-2000-S, LIGHTWAVE SUCTION ABLATOR, MODEL IA-2000-S, LIGHTWAVEFebruary 25, 2009
K060198MICROPOWER HAND PIECE : MEDIUM SPEED DRILL, SAGGITAL SAW, RECIPROCATING SAW, AND OSCILLATING SAWMay 11, 2006
K060260MICROPOWER HAND PIECE HIGH SPEED DRILLApril 10, 2006
K060270MICROPOWER HAND PIECE: ORAL MAX HIGH SPEED DRILLApril 10, 2006
K050519ADVANCED TURBO DRIVE SYSTEMMay 17, 2005
K050497BIOSCREW XTRALOK, 8X35MM & 8X40MM VIOLETMarch 25, 2005
K050227THREVO SUTURE ANCHOR WITH DISPOSABLE DRIVERMarch 2, 2005
K043106PINN-ACL CROSSPINJanuary 19, 2005
K042778BIOANCHOR WITH DISPOSABLE DRIVER, PRELOADED WITH ONE #2 HERCULINE SUTURENovember 4, 2004
K041128SUTURE ARROWJuly 29, 2004
K041713SUPER REVO HERCULINE SUTURE ANCHORJuly 22, 2004
K033573LINVATEC 10K IRRIGATION SYSTEMFebruary 11, 2004
K033804BIOANCHOR WITH DISPOSABLE DRIVERDecember 31, 2003
K033748TRIDENT RESECTION ABLATORDecember 15, 2003
K032607POWERPRO PNEUMATIC SYSTEM, MODELS PRO6150, PRO6175, PRO6185November 10, 2003
K031994LINVATEC 300W XENON LIGHT SOURCEAugust 21, 2003