FDA Browser
by
Innolitics
Anesthesiology
Review Panel
Cardiovascular
Review Panel
Miscellaneous
Miscellaneous
Subpart B—Cardiovascular Diagnostic Devices
CFR Sub-Part
Subpart B—Diagnostic Devices
CFR Sub-Part
Subpart C—Cardiovascular Monitoring Devices
CFR Sub-Part
Subpart D—Cardiovascular Prosthetic Devices
CFR Sub-Part
DST
Clip, Vena-Cava
2
Product Code
DSW
Bag, Polymeric Mesh, Pacemaker
1
Product Code
DSY
Prosthesis, Vascular Graft, Of 6mm And Greater Diameter
2
Product Code
DSZ
Pacemaker Battery
3
Product Code
DTA
Tester, Pacemaker Electrode Function
2
Product Code
DTB
Permanent Pacemaker Electrode
3
Product Code
P
13
0012
MYOPORE SUTURELESS MYOCARDIAL PACING LEAD
APPR
PMA Approval
P
12
0017
MODEL 5071 LEAD
APPR
PMA Approval
K
06
1212
BIOTRONIK ENDOCARDIAL PACING LEADS
3
Cleared 510(K)
K
04
1809
PERMANENT PACING LEAD, MODEL PY2
3
Cleared 510(K)
K
04
0569
PERMANENT PACING LEAD, MODEL REFINO, MODEL: REFINO-R, RU, RJU
3
Cleared 510(K)
K
03
1274
MODEL 5071 MYOCARDIAL PACING LEAD
3
Cleared 510(K)
K
03
1210
MODEL 4951M MYOCARDIAL UNIPOLAR LEAD
3
Cleared 510(K)
K
02
3205
ELOX P 45-BP; ELOX P 53-BP; ELOX P 60-BP
3
Cleared 510(K)
K
02
4053
PERMANENT PACING LEADS, MODELS PHYSIQUE PB AND PJB
3
Cleared 510(K)
K
02
3803
MODIFICATION TO BIOTRONIK'S STERILIZATION PROCESS
3
Cleared 510(K)
Show All 490 Submissions
DTC
Analyzer, Pacemaker Generator Function
2
Product Code
DTD
Pacemaker Lead Adaptor
2
Product Code
DTE
Pulse-Generator, Pacemaker, External
2
Product Code
DTF
Tools, Pacemaker Service
1
Product Code
DTG
Magnet, Test, Pacemaker
1
Product Code
DTI
Sizer, Heart-Valve, Prosthesis
1
Product Code
DTJ
Holder, Heart-Valve, Prosthesis
1
Product Code
DTK
Filter, Intravascular, Cardiovascular
2
Product Code
DSP
System, Balloon, Intra-Aortic And Control
2
Product Code
DSR
Stimulator, Carotid Sinus Nerve
3
Product Code
DSS
Clip, Vascular
2
Product Code
DXY
Implantable Pacemaker Pulse-Generator
3
Product Code
DXZ
Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene
2
Product Code
DYE
Replacement Heart-Valve
3
Product Code
DYF
Prosthesis, Vascular Graft, Of Less Then 6mm Diameter
2
Product Code
KFJ
Materials, Repair Or Replacement, Pacemaker
3
Product Code
KRD
Device, Vascular, For Promoting Embolization
2
Product Code
KRE
Analyzer, Pacemaker Generator Function, Indirect
2
Product Code
KRF
Charger, Pacemaker
1
Product Code
KRG
Programmer, Pacemaker
3
Product Code
KRH
Ring, Annuloplasty
2
Product Code
LDF
Electrode, Pacemaker, Temporary
2
Product Code
MAB
Marker, Cardiopulmonary Bypass (Vein Marker)
2
Product Code
MAL
Graft, Vascular, Synthetic/Biologic Composite
2
Product Code
MFX
Vessel Guard Or Cover, To Facilitate Revision Surgeries
2
Product Code
MOP
Rotator, Prosthetic Heart Valve
1
Product Code
MZY
Graft, Vascular, Stainless Steel Tunneler
2
Product Code
NHW
Electrode, Pacing And Cardioversion, Temporary, Epicardial
2
Product Code
NKO
System, Balloon, Intra-Aortic And Control, Reprocessed
3
Product Code
OKR
Ventricular Bypass (Assist) Device
3
Product Code
OMH
Pericardial Patch To Facilitate Revision Surgeries
2
Product Code
OMR
Vessel Guard Or Cover
2
Product Code
OTD
Endovascular Suturing System
2
Product Code
OVJ
Pulse Generator, External Pacemaker, Dual Chamber
2
Product Code
PAL
Pulmonic Replacement Heart Valve
F
Product Code
PCK
Pediatric Ventricular Assist Device
F
Product Code
PNJ
Leadless Pacemaker
3
Product Code
PNS
Short-Term Intravascular Filter Catheter
2
Product Code
PSQ
Intracardiac Patch Or Pledget, Biologically Derived
2
Product Code
PST
Aortic Annuloplasty Ring
2
Product Code
QAB
Pacing System Analyzer
2
Product Code
Subpart E—Cardiovascular Surgical Devices
CFR Sub-Part
Subpart E—Surgical Devices
CFR Sub-Part
Subpart F—Cardiovascular Therapeutic Devices
CFR Sub-Part
Subpart F—Therapeutic Devices
CFR Sub-Part
Chemistry
Review Panel
Dental
Review Panel
Ear, Nose, Throat
Review Panel
Gastroenterology and Urology
Review Panel
General Hospital
Review Panel
Hematology
Review Panel
Immunology
Review Panel
Microbiology
Review Panel
Neurology
Review Panel
Obstetrical and Gynecological
Review Panel
Ophthalmic
Review Panel
Orthopedic
Review Panel
Pathology
Review Panel
Physical Medicine
Review Panel
Radiology
Review Panel
General and Plastic Surgery
Review Panel
Toxicology
Review Panel
Medical Genetics
Review Panel
Unknown
Review Panel
Last synced on 9 May 2025 at 11:05 pm
CV
/
subpart-d—cardiovascular-prosthetic-devices
/
DTB
/
K023205
View Source
ELOX P 45-BP; ELOX P 53-BP; ELOX P 60-BP
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023205
510(k) Type
Traditional
Applicant
BIOTRONIK, INC.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
4/24/2003
Days to Decision
211 days
FDA Browser
by
Innolitics
Anesthesiology
Cardiovascular
Miscellaneous
Subpart B—Cardiovascular Diagnostic Devices
Subpart B—Diagnostic Devices
Subpart C—Cardiovascular Monitoring Devices
Subpart D—Cardiovascular Prosthetic Devices
DST
Clip, Vena-Cava
DSW
Bag, Polymeric Mesh, Pacemaker
DSY
Prosthesis, Vascular Graft, Of 6mm And Greater Diameter
DSZ
Pacemaker Battery
DTA
Tester, Pacemaker Electrode Function
DTB
Permanent Pacemaker Electrode
P
13
0012
MYOPORE SUTURELESS MYOCARDIAL PACING LEAD
P
12
0017
MODEL 5071 LEAD
K
06
1212
BIOTRONIK ENDOCARDIAL PACING LEADS
K
04
1809
PERMANENT PACING LEAD, MODEL PY2
K
04
0569
PERMANENT PACING LEAD, MODEL REFINO, MODEL: REFINO-R, RU, RJU
K
03
1274
MODEL 5071 MYOCARDIAL PACING LEAD
K
03
1210
MODEL 4951M MYOCARDIAL UNIPOLAR LEAD
K
02
3205
ELOX P 45-BP; ELOX P 53-BP; ELOX P 60-BP
K
02
4053
PERMANENT PACING LEADS, MODELS PHYSIQUE PB AND PJB
K
02
3803
MODIFICATION TO BIOTRONIK'S STERILIZATION PROCESS
Show All 490 Submissions
DTC
Analyzer, Pacemaker Generator Function
DTD
Pacemaker Lead Adaptor
DTE
Pulse-Generator, Pacemaker, External
DTF
Tools, Pacemaker Service
DTG
Magnet, Test, Pacemaker
DTI
Sizer, Heart-Valve, Prosthesis
DTJ
Holder, Heart-Valve, Prosthesis
DTK
Filter, Intravascular, Cardiovascular
DSP
System, Balloon, Intra-Aortic And Control
DSR
Stimulator, Carotid Sinus Nerve
DSS
Clip, Vascular
DXY
Implantable Pacemaker Pulse-Generator
DXZ
Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene
DYE
Replacement Heart-Valve
DYF
Prosthesis, Vascular Graft, Of Less Then 6mm Diameter
KFJ
Materials, Repair Or Replacement, Pacemaker
KRD
Device, Vascular, For Promoting Embolization
KRE
Analyzer, Pacemaker Generator Function, Indirect
KRF
Charger, Pacemaker
KRG
Programmer, Pacemaker
KRH
Ring, Annuloplasty
LDF
Electrode, Pacemaker, Temporary
MAB
Marker, Cardiopulmonary Bypass (Vein Marker)
MAL
Graft, Vascular, Synthetic/Biologic Composite
MFX
Vessel Guard Or Cover, To Facilitate Revision Surgeries
MOP
Rotator, Prosthetic Heart Valve
MZY
Graft, Vascular, Stainless Steel Tunneler
NHW
Electrode, Pacing And Cardioversion, Temporary, Epicardial
NKO
System, Balloon, Intra-Aortic And Control, Reprocessed
OKR
Ventricular Bypass (Assist) Device
OMH
Pericardial Patch To Facilitate Revision Surgeries
OMR
Vessel Guard Or Cover
OTD
Endovascular Suturing System
OVJ
Pulse Generator, External Pacemaker, Dual Chamber
PAL
Pulmonic Replacement Heart Valve
PCK
Pediatric Ventricular Assist Device
PNJ
Leadless Pacemaker
PNS
Short-Term Intravascular Filter Catheter
PSQ
Intracardiac Patch Or Pledget, Biologically Derived
PST
Aortic Annuloplasty Ring
QAB
Pacing System Analyzer
Subpart E—Cardiovascular Surgical Devices
Subpart E—Surgical Devices
Subpart F—Cardiovascular Therapeutic Devices
Subpart F—Therapeutic Devices
Chemistry
Dental
Ear, Nose, Throat
Gastroenterology and Urology
General Hospital
Hematology
Immunology
Microbiology
Neurology
Obstetrical and Gynecological
Ophthalmic
Orthopedic
Pathology
Physical Medicine
Radiology
General and Plastic Surgery
Toxicology
Medical Genetics
Unknown
CV
/
subpart-d—cardiovascular-prosthetic-devices
/
DTB
/
K023205
View Source
ELOX P 45-BP; ELOX P 53-BP; ELOX P 60-BP
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023205
510(k) Type
Traditional
Applicant
BIOTRONIK, INC.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
4/24/2003
Days to Decision
211 days