Biomet Microfixation RibFix Blu Thoracic Fixation System
K-Number: K162974 · 2016-12-09
Device Summary
Frequently Asked Questions
What is the Biomet Microfixation RibFix Blu Thoracic Fixation System?
Biomet Microfixation RibFix Blu Thoracic Fixation System is a medical device that received FDA 510(k) clearance on 2016-12-09. The listed applicant is Biomet Microfixation. The 510(k) number is K162974.
When did Biomet Microfixation RibFix Blu Thoracic Fixation System receive FDA 510(k) clearance?
Biomet Microfixation RibFix Blu Thoracic Fixation System received FDA 510(k) clearance on 2016-12-09, under 510(k) number K162974.
Who is the listed applicant for Biomet Microfixation RibFix Blu Thoracic Fixation System?
The FDA 510(k) record lists Biomet Microfixation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Biomet Microfixation RibFix Blu Thoracic Fixation System?
The FDA product code for Biomet Microfixation RibFix Blu Thoracic Fixation System is HRS.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Biomet Microfixation as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: HRS)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.