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FDA 510(k)

TRINICA ANTERIOR LUMBAR PLATE SYSTEM

K-Number: K061353 · 2006-08-30

ApplicantZimmer Spine, Inc.
Decision Date2006-08-30
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TRINICA ANTERIOR LUMBAR PLATE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer Spine, Inc.. It received FDA 510(k) clearance on 2006-08-30 under 510(k) number K061353. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRINICA ANTERIOR LUMBAR PLATE SYSTEM?

TRINICA ANTERIOR LUMBAR PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2006-08-30. The listed applicant is Zimmer Spine, Inc.. The 510(k) number is K061353.

When did TRINICA ANTERIOR LUMBAR PLATE SYSTEM receive FDA 510(k) clearance?

TRINICA ANTERIOR LUMBAR PLATE SYSTEM received FDA 510(k) clearance on 2006-08-30, under 510(k) number K061353.

Who is the listed applicant for TRINICA ANTERIOR LUMBAR PLATE SYSTEM?

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

What is the FDA product code for TRINICA ANTERIOR LUMBAR PLATE SYSTEM?

The FDA product code for TRINICA ANTERIOR LUMBAR PLATE SYSTEM is KWQ.

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Other records listing Zimmer Spine, Inc. as applicant

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Related Devices (Code: KWQ)

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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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