SELECT SHOULDER KEELED ALL-POLY GLENOIDS
K-Number: K962238 · 1996-08-09
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Device Summary
Frequently Asked Questions
What is the SELECT SHOULDER KEELED ALL-POLY GLENOIDS?
SELECT SHOULDER KEELED ALL-POLY GLENOIDS is a medical device that received FDA 510(k) clearance on 1996-08-09. The listed applicant is Intermedics Orthopedics. The 510(k) number is K962238.
When did SELECT SHOULDER KEELED ALL-POLY GLENOIDS receive FDA 510(k) clearance?
SELECT SHOULDER KEELED ALL-POLY GLENOIDS received FDA 510(k) clearance on 1996-08-09, under 510(k) number K962238.
Who is the listed applicant for SELECT SHOULDER KEELED ALL-POLY GLENOIDS?
The FDA 510(k) record lists Intermedics Orthopedics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SELECT SHOULDER KEELED ALL-POLY GLENOIDS?
The FDA product code for SELECT SHOULDER KEELED ALL-POLY GLENOIDS 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 Intermedics Orthopedics 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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