FDA 510(k) Applications Submitted by DAN W. MILLER

FDA 510(k) Number Submission Date Device Name Applicant
K111671 06/15/2011 SEASPINE MONOPOLAR PROBE SYSYEM SEASPINE, INC.
K102026 07/19/2010 SEASPINE SPACER SYSTEM SEASPINE, INC.
K112206 08/01/2011 CARDIFF ANTERIOR CERVICAL PLATE SYSTEM SEASPINE, INC.
K133752 12/09/2013 SONENDO OMNICLEAN ENDOTHERPAY SYSTEM CONSOLE, SONENDO OMNICLEAN MOLAR PROCEDURE KIT SONENDO, INC.
K130025 01/03/2013 SONENDO ENDOTHERAPY SYSTEM SONENDO, INC.
K970051 01/07/1997 MUSCLESENSE II CLINICAL ELECTROMYOGRAPHY DEVICE SMITH AND NEPHEW DONJOY, INC.
K970533 02/12/1997 MODEL 1100 COLD THERAPY DEVICE SMITH & NEPHEW, INC.
K991254 04/13/1999 QS DELIVERY SYSTEM SUB-Q, INC.
K962462 06/25/1996 MUSCLEMAX PLUS ELECTRICAL MUSCLE STIMULATOR SMITH AND NEPHEW DONJOY, INC.
K963489 09/03/1996 WHEEL CHAIR ACCESSORY SMITH AND NEPHEW DONJOY, INC.
K963490 09/03/1996 PROTECTIVE RESTRAINT - BELTS SMITH AND NEPHEW DONJOY, INC.
K963492 09/03/1996 PROTECTIVE RESTRAINT SMITH AND NEPHEW DONJOY, INC.
K955057 11/06/1995 MODEL 1100 COLD THERAPY DEVICE SMITH AND NEPHEW DONJOY, INC.
K965073 12/19/1996 9 X 25MM STANDARD INTERFERNECE SCRE (S.I.S.) ACL SCREW SMITH & NEPHEW, INC.
K160905 04/01/2016 Sonendo GentleWave System SONENDO, INC.
K153157 11/02/2015 Sonendo Gentle Wave System SONENDO, INC.


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