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FDA 510(k) Applications Submitted by Craig Corrance
FDA 510(k) Number
Submission Date
Device Name
Applicant
K000232
01/27/2000
ROTAGLIDE + MODULAR KNEE SYSTEM WITH FIXED MENISCUS
CORIN U.S.A.
K980545
02/12/1998
THE NUFFIELD TOTAL KNEE SYSTEM
CORIN U.S.A.
K990657
03/01/1999
TRIFIX PEDICLE SPINAL SCREW ASSEMBLY
CORIN U.S.A.
K992234
07/02/1999
THE TAPER-FIT TOTAL HIP SYSTEM
CORIN U.S.A.
K992235
07/02/1999
ZYRANOX ZIRCONIA CERAMIC FEMORAL HEADS
CORIN U.S.A.
K973005
08/13/1997
THE CORIFIX LIGAMENT ANCHOR
CORIN U.S.A.
K973231
08/27/1997
THE CORIFIX DYNAMIC HIP SCREW SYSTEM
CORIN U.S.A.
K142388
08/27/2014
Neo Total Knee System
New Era Orthopedics, LLC
K973425
09/10/1997
THE MEHDIAN LUMBO-SACRAL PEDICLE SCREW SYSTEM
CORIN U.S.A.
K973595
09/22/1997
THE POSTERIOR STABILISED NUFFIELD TOTAL KNEE SYSTEM
CORIN U.S.A.
K994152
12/08/1999
THE LIGAMENT ANCHOR SOFT SCREW
CORIN U.S.A.
K994153
12/08/1999
CORMET 2000 HEMI HIP METALLIC RESURFACING PROSTHESIS
CORIN U.S.A.
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