GLENOID RESURFACE COMPONENT PMN 3M
K-Number: K831234 · 1983-06-02
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Device Summary
Frequently Asked Questions
What is the GLENOID RESURFACE COMPONENT PMN 3M?
GLENOID RESURFACE COMPONENT PMN 3M is a medical device that received FDA 510(k) clearance on 1983-06-02. The listed applicant is 3M Company. The 510(k) number is K831234.
When did GLENOID RESURFACE COMPONENT PMN 3M receive FDA 510(k) clearance?
GLENOID RESURFACE COMPONENT PMN 3M received FDA 510(k) clearance on 1983-06-02, under 510(k) number K831234.
Who is the listed applicant for GLENOID RESURFACE COMPONENT PMN 3M?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GLENOID RESURFACE COMPONENT PMN 3M?
The FDA product code for GLENOID RESURFACE COMPONENT PMN 3M is KWT.
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 3M Company 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: KWT)
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.
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