FDA 510(k) Applications Submitted by LINDY KNISELY
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K110708 |
03/14/2011 |
EQUINOXE REVERSE SHOULDER COMPRESSION SCREW / 38MM AND 42MM GLENOSPHERE / SUPERIOR AUGMENT GLENOID PLATE, 10 DEGREES... |
EXACTECH, INC. |
K121067 |
04/06/2012 |
EXACTECH EQUINOXE SHOULDER SYSTEM TORQUE DEFINING SCREW AND SHORT REPLICATOR PLATE |
EXACTECH, INC. |
K121220 |
04/23/2012 |
EQUINOXE GLENOID, UHMWPE 16 PS=OSTERIOR AUGMENT PEGGED, SMALL, LEFT/RIGHT |
EXACTECH, INC. |
K121392 |
05/09/2012 |
NOVATION CROWN CUP LINERS; NEUTRAL, LIPPED, +5MM LATERALIZED, +5/10 DEGREE |
EXACTECH, INC. |
K103012 |
10/12/2010 |
EXACTECH BIOLOXDELTA / BIOLOX FEMORAL HEADS, 28MM OD, 32MM OD, 36MM OD, EXACTECH BIOLOX OPTION ADAPTERS/FEMORAL HEADS |
EXACTECH, INC. |
K093275 |
10/19/2009 |
EXACTECH EQUINOXE REVERSE SHOULDER SYSTEM 36MM GLENOSPHERE AND HUMERAL LINER |
EXACTECH, INC. |
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