Medical Device Network on MSN14d
FDA grants 510(k) clearance to Zimmer’s new revision knee implant component
The US Food and Drug Administration (FDA) has granted 510(k) clearance to Zimmer Biomet's new revision knee implant component ...
Zacks Small Cap Research on MSN4d
MGRM: Monogram Receives Clearance from the FDA on its 510(k) Submission for its mBôs TKA System.
MGRM READ THE FULL MGRM RESEARCH REPORT On March 17, 2025, Monogram (NASDAQ:MGRM) announced that the FDA has granted 510(k) clearance for its Monogram mBôs TKA System. This determination means that ...
Sacramento Bee7d
Monogram Technologies Announces FDA 510(k) Clearance for the Monogram mBôsTM TKA System
Ben Sexson, Monogram Chief Executive Officer, commented, "This FDA 510(k) clearance is a defining moment for Monogram. It marks the culmination of years of relentless effort, innovation ...
NeuroOne® Accelerates Timeline of 510(k) Submission to FDA for the OneRF® Trigeminal Nerve Ablation System to Treat Facial Pain
Submission for New Intended Use That Leverages Company’s Patented OneRF® Technology Platform Expected in May 2025 EDEN PRAIRIE, Minn., March 11, ...
Accelerate Diagnostics submits WAVE system for FDA 510(k) clearance
Accelerate Diagnostics (AXDX) announced the submission of its Accelerate WAVE system and positive blood culture gram-negative test kit to the ...