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FDA 510(k)

STRICKLAND TRAPEZIAL IMPLANT

K-Number: K951471 · 1995-08-09

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

Device Summary

STRICKLAND TRAPEZIAL IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 1995-08-09 under 510(k) number K951471. The device is classified under product code KYI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRICKLAND TRAPEZIAL IMPLANT?

STRICKLAND TRAPEZIAL IMPLANT is a medical device that received FDA 510(k) clearance on 1995-08-09. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K951471.

When did STRICKLAND TRAPEZIAL IMPLANT receive FDA 510(k) clearance?

STRICKLAND TRAPEZIAL IMPLANT received FDA 510(k) clearance on 1995-08-09, under 510(k) number K951471.

Who is the listed applicant for STRICKLAND TRAPEZIAL IMPLANT?

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 STRICKLAND TRAPEZIAL IMPLANT?

The FDA product code for STRICKLAND TRAPEZIAL IMPLANT is KYI.

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Related Devices (Code: KYI)

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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