BePOD Cannulated Arthrodesis Screws
K-Number: K170040 · 2017-04-04
ApplicantFournitures Hospitalieres Industrie
Decision Date2017-04-04
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
BePOD Cannulated Arthrodesis Screws is a medical device manufactured by Fournitures Hospitalieres Industrie. It received FDA 510(k) clearance on 2017-04-04 under approval number K170040. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the BePOD Cannulated Arthrodesis Screws?
BePOD Cannulated Arthrodesis Screws is a medical device that received FDA 510(k) clearance on 2017-04-04. It is manufactured by Fournitures Hospitalieres Industrie. The 510(k) number is K170040.
When was BePOD Cannulated Arthrodesis Screws approved by the FDA?
BePOD Cannulated Arthrodesis Screws received FDA 510(k) clearance on 2017-04-04, under approval number K170040.
What company makes BePOD Cannulated Arthrodesis Screws?
BePOD Cannulated Arthrodesis Screws is manufactured by Fournitures Hospitalieres Industrie.
What is the FDA product code for BePOD Cannulated Arthrodesis Screws?
The FDA product code for BePOD Cannulated Arthrodesis Screws is HWC. This falls under the Cardiovascular category.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.