SYNERGY ADJUSTABLE LENGTH ROD
K-Number: K990057 · 1999-06-28
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Device Summary
Frequently Asked Questions
What is the SYNERGY ADJUSTABLE LENGTH ROD?
SYNERGY ADJUSTABLE LENGTH ROD is a medical device that received FDA 510(k) clearance on 1999-06-28. The listed applicant is Interpore Cross Intl.. The 510(k) number is K990057.
When did SYNERGY ADJUSTABLE LENGTH ROD receive FDA 510(k) clearance?
SYNERGY ADJUSTABLE LENGTH ROD received FDA 510(k) clearance on 1999-06-28, under 510(k) number K990057.
Who is the listed applicant for SYNERGY ADJUSTABLE LENGTH ROD?
The FDA 510(k) record lists Interpore Cross Intl. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYNERGY ADJUSTABLE LENGTH ROD?
The FDA product code for SYNERGY ADJUSTABLE LENGTH ROD is MNI.
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 Interpore Cross Intl. 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: MNI)
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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