VITALITY HIP SYSTEM MODEL#420
K-Number: K070050 · 2007-05-23
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Device Summary
Frequently Asked Questions
What is the VITALITY HIP SYSTEM MODEL#420?
VITALITY HIP SYSTEM MODEL#420 is a medical device that received FDA 510(k) clearance on 2007-05-23. The listed applicant is Encore Medical L.P.. The 510(k) number is K070050.
When did VITALITY HIP SYSTEM MODEL#420 receive FDA 510(k) clearance?
VITALITY HIP SYSTEM MODEL#420 received FDA 510(k) clearance on 2007-05-23, under 510(k) number K070050.
Who is the listed applicant for VITALITY HIP SYSTEM MODEL#420?
The FDA 510(k) record lists Encore Medical L.P. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VITALITY HIP SYSTEM MODEL#420?
The FDA product code for VITALITY HIP SYSTEM MODEL#420 is LPH.
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 Encore Medical L.P. 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: LPH)
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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