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FDA 510(k)

SMITH & NEPHEW PORPS & TORPS

K-Number: K002737 · 2000-10-12

ApplicantGyrus Ent LLC
Decision Date2000-10-12
Product CodeETB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

SMITH & NEPHEW PORPS & TORPS is the device name listed in this FDA 510(k) record. The listed applicant is Gyrus Ent LLC. It received FDA 510(k) clearance on 2000-10-12 under 510(k) number K002737. The device is classified under product code ETB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMITH & NEPHEW PORPS & TORPS?

SMITH & NEPHEW PORPS & TORPS is a medical device that received FDA 510(k) clearance on 2000-10-12. The listed applicant is Gyrus Ent LLC. The 510(k) number is K002737.

When did SMITH & NEPHEW PORPS & TORPS receive FDA 510(k) clearance?

SMITH & NEPHEW PORPS & TORPS received FDA 510(k) clearance on 2000-10-12, under 510(k) number K002737.

Who is the listed applicant for SMITH & NEPHEW PORPS & TORPS?

The FDA 510(k) record lists Gyrus Ent LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SMITH & NEPHEW PORPS & TORPS?

The FDA product code for SMITH & NEPHEW PORPS & TORPS is ETB.

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Related Devices (Code: ETB)

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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