Medacta International
Medacta International holds FDA 510(k) medical device clearances, first cleared 2011, most recent 2016.
Top product codes for Medacta International
Recent clearances by Medacta International
- K160605 — MectaLIF Anterior Stand-Alone
- K160289 — MasterLoc Stem
- K153664 — M.U.S.T. Pedicle Screw System
- K151531 — MasterLoc Stem
- K142744 — Mecta-C TiPEEK
- K143453 — Mpact Double Mobility System
- K142069 — GMK EXTENSION
- K141988 — M.U.S.T PEDICLE SCREW SYSTEM
- K141044 — M.U.S.T. EXTENSION
- K140826 — GMK SPHERE EXTENSION
- K140361 — META-C CERVICAL PLATE
- K132788 — MYSPINE PEDICLE SCREW PLACEMENT GUIDES
- K133192 — MECTALIF TIPEEK
- K132879 — MPACT EXTENSION
- K133630 — GMK SHORT STEM
- K132878 — M.U.S.T. EXTENSION
- K131518 — MECTACER BIOLOX OPTION HEADS
- K131458 — MPACT DM LINER CONVERTER
- K131310 — GMK FULL PE TIBIAL COMPONENTS
- K130299 — GMK HINGE
- K123721 — GMK REVISION EXTENSION
- K131671 — MECTALIF
- K124034 — MECTALIF ANTERIOR
- K122911 — VERSAFITCUP CC TRIO EXTENSION
- K122232 — GMK NARROW
- K122641 — MPACT EXTENSION
- K121416 — GMK SPHERE
- K121115 — M.U.S.T PEDICLE SCREW SYSTEM
- K120790 — GMK - LINE EXTENSION
- K121011 — AMISTEM AND QUADRA - LINE EXTENSION
- K120531 — VERSAFITCUP CC TRIO-ADDITIONAL LINERS
- K113571 — GMK RESUFACING PATELLA SIZE 4
- K112862 — MECTA-C
- K112115 — MECTACER BIOLOX(R) DELTA FEMORAL HEADS
- K111145 — ENDO HEAD
- K110927 — MECTALIF
- K111283 — GMK REVISION HYBRID LINERS
- K103721 — MPACT ACETABULAR SYSTEM
- K103352 — VERSAFITCUP CC TRIO
Data sourced from openFDA. This site is unofficial and independent of the FDA.