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FDA 510(k)

SMITH & NEPHEW PISTONS

K-Number: K003214 · 2000-10-31

ApplicantGyrus Ent LLC
Decision Date2000-10-31
Product CodeETB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

SMITH & NEPHEW PISTONS 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 2000-10-31 under 510(k) number K003214. 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 PISTONS?

SMITH & NEPHEW PISTONS is a medical device that received FDA 510(k) clearance on 2000-10-31. The listed applicant is Gyrus Ent LLC. The 510(k) number is K003214.

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

SMITH & NEPHEW PISTONS received FDA 510(k) clearance on 2000-10-31, under 510(k) number K003214.

Who is the listed applicant for SMITH & NEPHEW PISTONS?

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 PISTONS?

The FDA product code for SMITH & NEPHEW PISTONS is ETB.

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Other records listing Gyrus Ent LLC as applicant

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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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

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