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FDA 510(k)

REPROCESSED DILATING TIP TROCARS

K-Number: K132629 · 2013-12-31

ApplicantStryker Sustainability Solutions
Decision Date2013-12-31
Product CodeNLM
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

REPROCESSED DILATING TIP TROCARS is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Sustainability Solutions. It received FDA 510(k) clearance on 2013-12-31 under 510(k) number K132629. The device is classified under product code NLM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPROCESSED DILATING TIP TROCARS?

REPROCESSED DILATING TIP TROCARS is a medical device that received FDA 510(k) clearance on 2013-12-31. The listed applicant is Stryker Sustainability Solutions. The 510(k) number is K132629.

When did REPROCESSED DILATING TIP TROCARS receive FDA 510(k) clearance?

REPROCESSED DILATING TIP TROCARS received FDA 510(k) clearance on 2013-12-31, under 510(k) number K132629.

Who is the listed applicant for REPROCESSED DILATING TIP TROCARS?

The FDA 510(k) record lists Stryker Sustainability Solutions as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REPROCESSED DILATING TIP TROCARS?

The FDA product code for REPROCESSED DILATING TIP TROCARS is NLM.

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Other records listing Stryker Sustainability Solutions as applicant

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Related Devices (Code: NLM)

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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