CREED Cannulated Screws
K-Number: K223847 · 2023-01-25
ApplicantGlw, Inc.
Decision Date2023-01-25
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
CREED Cannulated Screws is a medical device manufactured by Glw, Inc.. It received FDA 510(k) clearance on 2023-01-25 under approval number K223847. 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 CREED Cannulated Screws?
CREED Cannulated Screws is a medical device that received FDA 510(k) clearance on 2023-01-25. It is manufactured by Glw, Inc.. The 510(k) number is K223847.
When was CREED Cannulated Screws approved by the FDA?
CREED Cannulated Screws received FDA 510(k) clearance on 2023-01-25, under approval number K223847.
What company makes CREED Cannulated Screws?
CREED Cannulated Screws is manufactured by Glw, Inc..
What is the FDA product code for CREED Cannulated Screws?
The FDA product code for CREED Cannulated 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.