Linvatec Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Linvatec Corp. - FDA 510(k) Cleared Devices
Recent clearances: CONMED LINVATEC INTERCEPT IMPLANT, CONMED LINVATEC SOFT TISSUE TO BONE SYSTEM, CONMED LINVATEC BIO MINI-REVO SUTURE ANCHOR, MODEL C6170CR
93
Total
87
Cleared
0
Denied
Linvatec Corp. has 87 FDA 510(k) cleared medical devices. Based in Research Triangle Pa, US.
Historical record: 87 cleared submissions from 1992 to 2009. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Linvatec Corp. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Conmed Corporation as regulatory consultant.
FDA 510(k) Regulatory Record - Linvatec Corp.
93 devices
Cleared
Dec 23, 2009
CONMED LINVATEC INTERCEPT IMPLANT
Orthopedic
86d
Cleared
Jun 23, 2009
CONMED LINVATEC SOFT TISSUE TO BONE SYSTEM
Orthopedic
27d
Cleared
Jun 22, 2009
CONMED LINVATEC BIO MINI-REVO SUTURE ANCHOR, MODEL C6170CR
Orthopedic
87d
Cleared
Apr 10, 2009
CONMED LINVATEC PALADIN, PRELOADED WITH TWO #2 HI-FI SUTURES
Orthopedic
74d
Cleared
Feb 25, 2009
EL LIGHTWAVE SUCTION ABLATOR, MODEL EL-2000-S, LIGHTWAVE SUCTION ABLATOR,...
General & Plastic Surgery
110d
Cleared
May 11, 2006
MICROPOWER HAND PIECE : MEDIUM SPEED DRILL, SAGGITAL SAW, RECIPROCATING SAW,...
Orthopedic
105d
Cleared
Apr 10, 2006
MICROPOWER HAND PIECE HIGH SPEED DRILL
Neurology
68d
Cleared
Apr 10, 2006
MICROPOWER HAND PIECE: ORAL MAX HIGH SPEED DRILL
Dental
68d
Cleared
May 17, 2005
ADVANCED TURBO DRIVE SYSTEM
General & Plastic Surgery
77d
Cleared
Mar 25, 2005
BIOSCREW XTRALOK, 8X35MM & 8X40MM VIOLET
Orthopedic
25d
Cleared
Mar 02, 2005
THREVO SUTURE ANCHOR WITH DISPOSABLE DRIVER
Orthopedic
29d
Cleared
Jan 19, 2005
PINN-ACL CROSSPIN
Orthopedic
71d
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