FDA 510(k) Applications Submitted by DAN 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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