PMT Expandable Cage (PMT EXP)
K-Number: K230297 · 2023-08-11
ApplicantProvidence Medical Technology, Inc.
Decision Date2023-08-11
Product CodeMRW
DecisionSubstantially Equivalent
Device Summary
PMT Expandable Cage (PMT EXP) is a medical device manufactured by Providence Medical Technology, Inc.. It received FDA 510(k) clearance on 2023-08-11 under approval number K230297. The device is classified under product code MRW. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the PMT Expandable Cage (PMT EXP)?
PMT Expandable Cage (PMT EXP) is a medical device that received FDA 510(k) clearance on 2023-08-11. It is manufactured by Providence Medical Technology, Inc.. The 510(k) number is K230297.
When was PMT Expandable Cage (PMT EXP) approved by the FDA?
PMT Expandable Cage (PMT EXP) received FDA 510(k) clearance on 2023-08-11, under approval number K230297.
What company makes PMT Expandable Cage (PMT EXP)?
PMT Expandable Cage (PMT EXP) is manufactured by Providence Medical Technology, Inc..
What is the FDA product code for PMT Expandable Cage (PMT EXP)?
The FDA product code for PMT Expandable Cage (PMT EXP) is MRW.
Other Devices by Providence Medical Technology, Inc.
Related Devices (Code: MRW)
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.