IONICS LEVANTE INTERVERTEBRAL PILLAR, EXPANDABLE
K-Number: K983667 · 2000-07-05
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Device Summary
Frequently Asked Questions
What is the IONICS LEVANTE INTERVERTEBRAL PILLAR, EXPANDABLE?
IONICS LEVANTE INTERVERTEBRAL PILLAR, EXPANDABLE is a medical device that received FDA 510(k) clearance on 2000-07-05. The listed applicant is Ionics Medical Corp.. The 510(k) number is K983667.
When did IONICS LEVANTE INTERVERTEBRAL PILLAR, EXPANDABLE receive FDA 510(k) clearance?
IONICS LEVANTE INTERVERTEBRAL PILLAR, EXPANDABLE received FDA 510(k) clearance on 2000-07-05, under 510(k) number K983667.
Who is the listed applicant for IONICS LEVANTE INTERVERTEBRAL PILLAR, EXPANDABLE?
The FDA 510(k) record lists Ionics Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IONICS LEVANTE INTERVERTEBRAL PILLAR, EXPANDABLE?
The FDA product code for IONICS LEVANTE INTERVERTEBRAL PILLAR, EXPANDABLE is MQP.
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 Ionics Medical Corp. 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: MQP)
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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