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510(k) Premarket Notification - Food and Drug …
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K130089
- 510 (k) Premarket Notification FDA Home Medical Devices Databases 510 (k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards …
510(k) Premarket Notification
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K133372
- 510 (k) Premarket Notification FDA Home Medical Devices Databases 510 (k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards …
510(k) Premarket Notification
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?start_search=211&ProductCode=&KNumber=&Applicant=&DeviceName=&Type=&ClinicalTrials=off&DecisionDateTo=06%2F11%2F2022&Redact510K=&CombinationProducts=&ZNumber=&SortColumn=an%5Fasc
- 510(K) Number. Decision Date. crosstrees pva pod: CROSSTREES MEDICAL, INC. K133372: 12/06/2013 crosstrees pva pod: CROSSTREES MEDICAL, INC. K130089: …
510(k) Premarket Notification
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?start_search=191&ProductCode=&KNumber=&Applicant=&DeviceName=&Type=&ClinicalTrials=off&DecisionDateTo=10%2F15%2F2021&Redact510K=&CombinationProducts=&ZNumber=&SortColumn=kn%5Fasc
- 510(K) Number. Decision Date. ulthera system: ULTHERA, INC. K134032: 06/20/2014 crosstrees pva pod: CROSSTREES MEDICAL, INC. K133372: 12/06/2013 sjm confirm …
113 - Food and Drug Administration
- https://www.accessdata.fda.gov/cdrh_docs/pdf13/K130089.pdf
- Submitter's Name: Crosstrees Medical, Inc. Address: 4735 Walnut Street, Suite E Boulder, CO 80301 Telephone: 720-880-5811 Fax: 303-484-6099 Contact Person: Robert Scribner …
Search the Releasable 510(k) Database | FDA
- https://www.fda.gov/medical-devices/510k-clearances/search-releasable-510k-database
- You can search the releasable 510 (k) database by Panel, 510 (k) number, Product code or Device name. A search query will produce information from the database in the following …
Crosstrees Medical secures FDA 510(k) approval for its PVA pod …
- https://www.medicaldevice-network.com/uncategorized/newscrosstrees-medical-secures-fda-510k-approval-for-its-pva-pod-system/
- Medical Devices. Anesthesia and Respiratory Devices; Cardiovascular; Dental Devices; Diabetes Care Devices; Nephrology and Urology Devices; Neurology …
Crosstrees Medical Gets FDA 510(k) Nod for Next Generation
- https://www.biospace.com/article/releases/crosstrees-medical-gets-fda-510-k-nod-for-next-generation-device-for-percutaneous-vertebral-augmentation-pva-/
- The Crosstrees® Pod technology was designed to address the need for improved vertebral fracture repair devices by taking a novel approach to controlling the …
510(k) Clearances | FDA - U.S. Food and Drug …
- https://www.fda.gov/medical-devices/device-approvals-denials-and-clearances/510k-clearances
- 510 (k) Clearances 510 (k) Clearances Overview Section 510 (k) of the Food, Drug and Cosmetic Act requires device manufacturers who must register, to notify FDA of …
Crosstrees Medical obtains FDA 510(k) approval for Crosstrees …
- https://www.nsmedicaldevices.com/news/crosstrees-medical-obtains-fda-510k-approval-for-crosstrees-pva-pod-system-200913/
- The FDA approval for the CE marked Crosstrees PVA pod system is based on a prospective, single-arm IDE study, which showed significant reduction in pain scores …
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