Linvatec Corp.
FDA 510(k) medical device clearances.
Top product codes for Linvatec Corp.
Recent clearances by Linvatec Corp.
- K092998 — CONMED LINVATEC INTERCEPT IMPLANT
- K091549 — CONMED LINVATEC SOFT TISSUE TO BONE SYSTEM
- K090835 — CONMED LINVATEC BIO MINI-REVO SUTURE ANCHOR, MODEL C6170CR
- K090186 — CONMED LINVATEC PALADIN, PRELOADED WITH TWO #2 HI-FI SUTURES
- K083281 — EL LIGHTWAVE SUCTION ABLATOR, MODEL EL-2000-S, LIGHTWAVE SUCTION ABLATOR, MODEL IA-2000-S, LIGHTWAVE ABLATOR, MODEL IA-
- K060198 — MICROPOWER HAND PIECE : MEDIUM SPEED DRILL, SAGGITAL SAW, RECIPROCATING SAW, AND OSCILLATING SAW
- K060260 — MICROPOWER HAND PIECE HIGH SPEED DRILL
- K060270 — MICROPOWER HAND PIECE: ORAL MAX HIGH SPEED DRILL
- K050519 — ADVANCED TURBO DRIVE SYSTEM
- K050497 — BIOSCREW XTRALOK, 8X35MM & 8X40MM VIOLET
- K050227 — THREVO SUTURE ANCHOR WITH DISPOSABLE DRIVER
- K043106 — PINN-ACL CROSSPIN
- K042778 — BIOANCHOR WITH DISPOSABLE DRIVER, PRELOADED WITH ONE #2 HERCULINE SUTURE
- K041128 — SUTURE ARROW
- K041713 — SUPER REVO HERCULINE SUTURE ANCHOR
- K033573 — LINVATEC 10K IRRIGATION SYSTEM
- K033804 — BIOANCHOR WITH DISPOSABLE DRIVER
- K033748 — TRIDENT RESECTION ABLATOR
- K032607 — POWERPRO PNEUMATIC SYSTEM, MODELS PRO6150, PRO6175, PRO6185
- K031994 — LINVATEC 300W XENON LIGHT SOURCE
- K031098 — 3-CCD DIGITAL CAMERA SYSTEM
- K030720 — ULTRABLATOR ELECTRODE
- K022827 — ULTRAFIX KNOTLESS MINIMITE SUTURE ANCHOR
- K013131 — BIOSCREW XTRALOK
- K020377 — PRE-LOADED BIOSTINGER HORNET
- K013369 — RESECTION ABLATOR
- K013553 — PRE-LOADED ULTRAFIX RC
- K013117 — RESECTION ABLATOR
- K012320 — POWERPRO BATTERY SYSTEM
- K003984 — SUPER REVO SUTURE ANCHOR
- K002088 — SHAVER ABLATOR
- K002523 — ADVANTAGE DRIVE SYSTEM
- K993885 — ULTRABLATOR ELECTRODE
- K993339 — ENDOPEARL WITH THREADER
- K991024 — BONE BULLET SUTURE ANCHOR
- K990194 — BIOBUTTON
- K991830 — CAPSULAR SHRINKAGE ELECTRODE
- K991715 — BIOSTINGER-V BIOABSORBABLE MENISCAL REPAIR DEVICE
- K990770 — BIORC ANCHOR
- K990524 — E9000 SYSTEM
- K984171 — ENDOPEARL
- K983652 — ABLATOR ELECTRODE
- K983186 — BIO-ANCHOR, PRE-LOADED BIOABSORBABLE SUTURE ANCHOR
- K981636 — INTEGRATED DRIVE/PUMP SYSTEM
- K981692 — MENISCAL REPAIR DEVICE
- K981637 — INTEGRATED DRIVE/PUMP SYSTEM FOR OTOLARYNGOLOGY
- K981269 — UNIVERSAL DRIVE SYSTEM
- K974538 — MENISCAL REPAIR DEVICE
- K973758 — BIOSCREW ABSORBABLE INTERFERENCE SREW
- K963932 — PRELOADED SOFT TISSUE ANCHOR
- K971059 — UNIVERSAL DRIVE SYSTEM
- K964805 — BIO-ANCHOR
- K963369 — BIO-ANCHOR
- K964548 — APEX UNIVERSAL DRIVE SYSTEM
- K960652 — BIOSCREW ABSORBABLE INTERFERENCE SCREW
- K961590 — APEX UNIVERSAL IRRIGATION SYSTEM & TWO-CONNECTION TUBING SET
- K960962 — INTERFERENCE SCREW
- K960940 — BIOSCREW ABSORBABLE INTERFERENCE SCREW
- K961192 — IRRIGATION SYSTEM
- K960852 — HALL MODULAR ACETABULAR REAMER SYSTEM
- K955486 — BIO-ANCHOR
- K953954 — PRELOADED SOFT TISSUE ANCHOR
- K954682 — WASHER, BOLT, NUT, ORTHOPEDIC
- K955273 — CANNULOC THREADED CANNULA
- K954440 — APEX TUBING SET
- K953702 — WASHER
- K952831 — BIOSCREW ABSORBABLE INTERFERENCE SCREW
- K944553 — PRESSURE SENSING SCOPE SHEATH SYSTEM
- K941862 — INTEQ TFCC REPAIR SYSTEM
- K934321 — LINVATEC STASYS-PES FIXATION DEVICE
- K944992 — ELECTRODES
- K951263 — INTRAARC DRIVE SYSTEM
- K941651 — CTS RELIEF KIT
- K933873 — CONCEPT UNIVERSAL PUMP SYSTEM
- K942447 — HASSON OPEN LAPAROSCOPY CANNULA
- K944476 — APEX UNIVERSAL DRIVE SYSTEM
- K942080 — SENSATEC ENDOSCOPIC INSTRUMENTS
- K942077 — BI-TEC ENDOSCOPIC BIPOLAR INSTRUMENTS
- K943985 — LIMITED REUSE BLADES
- K941691 — REVO ROTATOR CUFF REPAIR SYSTEM
- K941711 — HYPERFLEX FLEXIBLE GUIDEWIRES
- K942484 — VERRES NEEDLE
- K942414 — TROCAR SLEEVE, SEALING CAPS, REDUCER, LOOP GUIDE
- K922420 — CONTINUOUS FLOW HYSTERO-RESECTOSCOPE
- K942415 — R-BAR RETRACTOR
- K942416 — HASSON GRASPERS
- K940515 — POLY BLADES
- K933719 — BIOSCREW ABSORBABLE INTERFERENCE SCREW
- K934379 — LINVATEC POWERLINK SURGICAL SHAVING SYSTEM
- K933352 — CONCEPT CANNULATED INTEREFERENCE SCREW
- K932700 — CUTO(TM) TISSUE MORCELLATION SYSTEM
- K924941 — CONCEPT 4MM CANCELLOUS SCREW WITH EYELET
- K922186 — HEM-O-LOK -- MODIFICATION
Data sourced from openFDA. This site is unofficial and independent of the FDA.