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FDA 510(k)

SLT 28MM XXL FEMORAL HEAD

K-Number: K953025 · 1995-09-08

ApplicantWrightmedicaltechnologyinc
Decision Date1995-09-08
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SLT 28MM XXL FEMORAL HEAD is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 1995-09-08 under 510(k) number K953025. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SLT 28MM XXL FEMORAL HEAD?

SLT 28MM XXL FEMORAL HEAD is a medical device that received FDA 510(k) clearance on 1995-09-08. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K953025.

When did SLT 28MM XXL FEMORAL HEAD receive FDA 510(k) clearance?

SLT 28MM XXL FEMORAL HEAD received FDA 510(k) clearance on 1995-09-08, under 510(k) number K953025.

Who is the listed applicant for SLT 28MM XXL FEMORAL HEAD?

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

What is the FDA product code for SLT 28MM XXL FEMORAL HEAD?

The FDA product code for SLT 28MM XXL FEMORAL HEAD is JDI.

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Related Devices (Code: JDI)

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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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