JAX GRANULES BONE VOID FILLER
K-Number: K010557 · 2001-05-25
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Device Summary
Frequently Asked Questions
What is the JAX GRANULES BONE VOID FILLER?
JAX GRANULES BONE VOID FILLER is a medical device that received FDA 510(k) clearance on 2001-05-25. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K010557.
When did JAX GRANULES BONE VOID FILLER receive FDA 510(k) clearance?
JAX GRANULES BONE VOID FILLER received FDA 510(k) clearance on 2001-05-25, under 510(k) number K010557.
Who is the listed applicant for JAX GRANULES BONE VOID FILLER?
The FDA 510(k) record lists Smith & Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JAX GRANULES BONE VOID FILLER?
The FDA product code for JAX GRANULES BONE VOID FILLER is MQV.
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 Smith & Nephew, 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: MQV)
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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