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FDA 510(k) Applications Submitted by KLS MARTIN L.P.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K220050
01/06/2022
KLS Martin IPS Distraction
KLS Martin L.P.
K070169
01/18/2007
KLS MARTIN QUICK DISC, STERNAL TALON AND STERNAL PLATING - STERILE
KLS MARTIN L.P.
K060177
01/23/2006
KLS MARTIN RIGID FIXATION - STERILE
KLS MARTIN L.P.
K150771
03/24/2015
RxG Distraction System
KLS MARTIN L.P.
K151382
05/22/2015
Patient Contoured Implant-PEEK (PCI-PEEK)
KLS MARTIN L.P.
K141489
06/05/2014
LINOS MOH HAND PLATING SYSTEM
KLS MARTIN L.P.
K151983
07/17/2015
KLS Martin LSS Plating System
KLS MARTIN L.P.
K122860
09/18/2012
KLS MARTIN RECON TALON
KLS MARTIN L.P.
K062857
09/25/2006
KLS MARTIN QUICK DISC
KLS MARTIN L.P.
K221938
07/01/2022
KLS Martin Pure Pectus System
KLS Martin L.P.
K083432
11/20/2008
DRILL FREE MMF SCREW
KLS MARTIN L.P.
K072764
09/28/2007
KLS MARTIN XTERNAL FIXATOR
KLS MARTIN L.P.
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