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FDA 510(k)

NUVASIVE MESH

K-Number: K020853 · 2002-06-13

ApplicantNuvasive, Inc.
Decision Date2002-06-13
Product CodeEZX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NUVASIVE MESH is the device name listed in this FDA 510(k) record. The listed applicant is Nuvasive, Inc.. It received FDA 510(k) clearance on 2002-06-13 under 510(k) number K020853. The device is classified under product code EZX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NUVASIVE MESH?

NUVASIVE MESH is a medical device that received FDA 510(k) clearance on 2002-06-13. The listed applicant is Nuvasive, Inc.. The 510(k) number is K020853.

When did NUVASIVE MESH receive FDA 510(k) clearance?

NUVASIVE MESH received FDA 510(k) clearance on 2002-06-13, under 510(k) number K020853.

Who is the listed applicant for NUVASIVE MESH?

The FDA 510(k) record lists Nuvasive, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NUVASIVE MESH?

The FDA product code for NUVASIVE MESH is EZX.

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Other records listing Nuvasive, 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.

K240507NuVasive AttraX ScaffoldK223731NuVasive Modulus-C Interbody SystemK211757Simplify DiscK173117NuVasive® VersaTie™ SystemK133052AFFIX(R) NEXT GEN SPINOUS PROCESS PLATE SYSTEMK131025ARCHON ANTERIOR CERVICAL PLATE SYSTEM

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Related Devices (Code: EZX)

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.

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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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