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FDA 510(k) Applications Submitted by VIKKI M HOFFMAN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K020244
01/24/2002
SYNTHES THORACOLUMBAR SPINE LOCKING PLATE (TSLP)
SYNTHES SPINE
K030377
02/05/2003
MODIFICATION TO SYNTHES CERVIFIX SYSTEM
SYNTHES (USA)
K020517
02/19/2002
SYNTHES DUAL-OPENING USS
SYNTHES (USA)
K022791
08/22/2002
SYNTHES ANTERIOR TENSION BAND (ATB) SYSTEM
SYNTHES (USA)
K022949
09/05/2002
SYNTHES USS, CLICK'X, USS VAS, DUAL-OPENING USS AND SMALL STATURE USS
SYNTHES (USA)
K002849
09/13/2000
PRECISIONEDGE-ACC, PRECISIONEDGE-ACS, PRECISIONEDGE-LSK, AND PRECISIONEDGE-CB MICROKEATOME BLADES
SURGICAL SPECIALTIES CORP.
K003015
09/27/2000
SSC'S PCL MONOFILAMENT SAS, VIOLET, COATED, MODEL TBD
SURGICAL SPECIALTIES CORP.
K023675
11/01/2002
SYNTHES CERVIFIX/ AXON
SYNTHES (USA)
K023862
11/20/2002
NORIAN XR CALCIUM PHOSPHATE BONE VOID FILLER
SYNTHES (USA)
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