MODULAR PRESS FIT (MPF) STEM
K-Number: K855200 · 1986-04-01
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Device Summary
Frequently Asked Questions
What is the MODULAR PRESS FIT (MPF) STEM?
MODULAR PRESS FIT (MPF) STEM is a medical device that received FDA 510(k) clearance on 1986-04-01. The listed applicant is Depuy, Inc.. The 510(k) number is K855200.
When did MODULAR PRESS FIT (MPF) STEM receive FDA 510(k) clearance?
MODULAR PRESS FIT (MPF) STEM received FDA 510(k) clearance on 1986-04-01, under 510(k) number K855200.
Who is the listed applicant for MODULAR PRESS FIT (MPF) STEM?
The FDA 510(k) record lists Depuy, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODULAR PRESS FIT (MPF) STEM?
The FDA product code for MODULAR PRESS FIT (MPF) STEM is JDI.
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 Depuy, Inc. 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: JDI)
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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