Percutaneous - PDFSEARCH.IO - Document Search Engine

Percutaneous
Results: 1415

#	Item
911	BridgePoint Medical System CTO Indication K102725/S2 MAY[removed]K) SUMMARY This summary of 5 10(k) safety and effectiveness information is submitted in accordance Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2011-06-27 00:47:51 Port Balloon catheter Remote magnetic navigation Brivant Medicine Catheters Percutaneous
912	K\2$Z 510(k) Summary JUN -2 Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2011-07-25 00:34:49 Food and Drug Administration Catheters Port Medical device Percutaneous Federal Food Drug and Cosmetic Act Premarket approval Medicine Medical technology Medical equipment
913	B. Braun Interventional Systems Inc. Special 510(k) Premarket Notification (K[removed]Celsite(I) Implantable Access Port Systems APR[removed] Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-05-06 11:18:53 Surgery Food and Drug Administration Implants Port Intravenous therapy Percutaneous Federal Food Drug and Cosmetic Act Medical device Premarket approval Medicine Medical equipment Catheters
914	VJS405O 510(k) SUMMARY February 14, 2013 Name, Address, Phone and Fax Number of Applicant Teleflex Medical, Incorporated Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-12-09 11:45:15 Respiratory therapy Intensive care medicine First aid Cricothyrotomy Artificial airway Tracheotomy Airway management Tracheal intubation Percutaneous Medicine Medical equipment Emergency medicine
915	Kia34 Traditional 510(k) Bard PTV Dilatation Catheter Page 97 Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2012-12-06 10:13:31 Percutaneous Port Balloon catheter Medicine Catheters C. R. Bard
916 $Percutaneous vertebroplasty / Vertebral column / Compression fracture / Pathologic fracture / Bone cement / Osteoporosis / Vesselplasty / Medicine / Orthopedic surgery / Bone fractures$	510(k) Summary for the Cohesion Bone Cement In accordance with 21 CFR[removed]of the Federal Code of Regulations the following 510(k) summary is submitted for the Cohesion Bone Cement K 0 3 -( Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2011-03-07 11:37:25 Percutaneous vertebroplasty Vertebral column Compression fracture Pathologic fracture Bone cement Osteoporosis Vesselplasty Medicine Orthopedic surgery Bone fractures
917	Concentric Medical, Inc. Traditional 510(k) Submission, K131492 510(k) Summary Trade Name: Common Name: Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-11-14 08:33:13 Biocompatibility Predicate Package testing Percutaneous ISO 10993 Medicine Surgery Catheter
918	10o3 O 51 0(k) Summary SEP - Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2011-10-31 00:31:48 Interventional cardiology Implants Percutaneous coronary intervention Balloon catheter Angioplasty Catheter Coronary stent Stent Restenosis Medicine Interventional radiology Surgery
919	JAN 510(K) SUMMARY of SAFETY AND EFFECTIVENESS SPONSOR: N Volcano Corporation Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2012-02-27 00:30:52 Premarket approval Medical device Catheter Center for Devices and Radiological Health Percutaneous Title 21 of the Code of Federal Regulations Medicine Food and Drug Administration Health
920	TriReme Medical, Inc. Traditional 510(k) Premarket Notification (KI[removed]GliderTM PTCA Balloon Catheter[removed]k) Summary Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2012-04-23 00:32:55 Premarket approval Catheter Medical device Angioplasty Balloon catheter Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Percutaneous Medicine Food and Drug Administration Percutaneous coronary intervention

UPDATE