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FDA 510(k)

PDS PLATES

K-Number: K092590 · 2010-02-17

ApplicantETHICON, Inc.
Decision Date2010-02-17
Product CodeNHB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

PDS PLATES is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 2010-02-17 under 510(k) number K092590. The device is classified under product code NHB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PDS PLATES?

PDS PLATES is a medical device that received FDA 510(k) clearance on 2010-02-17. The listed applicant is ETHICON, Inc.. The 510(k) number is K092590.

When did PDS PLATES receive FDA 510(k) clearance?

PDS PLATES received FDA 510(k) clearance on 2010-02-17, under 510(k) number K092590.

Who is the listed applicant for PDS PLATES?

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

What is the FDA product code for PDS PLATES?

The FDA product code for PDS PLATES is NHB.

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Other records listing ETHICON, Inc. as applicant

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Related Devices (Code: NHB)

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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