FDA 510(k)

SLR-PLUS STANDARD AND LATERAL FEMORAL STEMS

K-Number: K093991 · 2010-04-15

Decision Date2010-04-15

Product CodeLZO

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

SLR-PLUS STANDARD AND LATERAL FEMORAL STEMS is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2010-04-15 under 510(k) number K093991. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SLR-PLUS STANDARD AND LATERAL FEMORAL STEMS?

SLR-PLUS STANDARD AND LATERAL FEMORAL STEMS is a medical device that received FDA 510(k) clearance on 2010-04-15. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K093991.

When did SLR-PLUS STANDARD AND LATERAL FEMORAL STEMS receive FDA 510(k) clearance?

SLR-PLUS STANDARD AND LATERAL FEMORAL STEMS received FDA 510(k) clearance on 2010-04-15, under 510(k) number K093991.

Who is the listed applicant for SLR-PLUS STANDARD AND LATERAL FEMORAL STEMS?

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

What is the FDA product code for SLR-PLUS STANDARD AND LATERAL FEMORAL STEMS?

The FDA product code for SLR-PLUS STANDARD AND LATERAL FEMORAL STEMS is LZO.

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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.