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FDA 510(k)

PINNACLETM Constrained Acetabular Liners

K-Number: K240639 · 2024-04-04

ApplicantDepuy Ireland UC
Decision Date2024-04-04
Product CodeKWZ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PINNACLETM Constrained Acetabular Liners is a medical device manufactured by Depuy Ireland UC. It received FDA 510(k) clearance on 2024-04-04 under approval number K240639. The device is classified under product code KWZ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PINNACLETM Constrained Acetabular Liners?

PINNACLETM Constrained Acetabular Liners is a medical device that received FDA 510(k) clearance on 2024-04-04. It is manufactured by Depuy Ireland UC. The 510(k) number is K240639.

When was PINNACLETM Constrained Acetabular Liners approved by the FDA?

PINNACLETM Constrained Acetabular Liners received FDA 510(k) clearance on 2024-04-04, under approval number K240639.

What company makes PINNACLETM Constrained Acetabular Liners?

PINNACLETM Constrained Acetabular Liners is manufactured by Depuy Ireland UC.

What is the FDA product code for PINNACLETM Constrained Acetabular Liners?

The FDA product code for PINNACLETM Constrained Acetabular Liners is KWZ.

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Related Devices (Code: KWZ)

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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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