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FDA 510(k)

MEDOFF SLIDING PLATE (PROPOSED NAME)

K-Number: K962251 · 1997-01-22

ApplicantWrightmedicaltechnologyinc
Decision Date1997-01-22
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MEDOFF SLIDING PLATE (PROPOSED NAME) is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 1997-01-22 under 510(k) number K962251. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDOFF SLIDING PLATE (PROPOSED NAME)?

MEDOFF SLIDING PLATE (PROPOSED NAME) is a medical device that received FDA 510(k) clearance on 1997-01-22. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K962251.

When did MEDOFF SLIDING PLATE (PROPOSED NAME) receive FDA 510(k) clearance?

MEDOFF SLIDING PLATE (PROPOSED NAME) received FDA 510(k) clearance on 1997-01-22, under 510(k) number K962251.

Who is the listed applicant for MEDOFF SLIDING PLATE (PROPOSED NAME)?

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 MEDOFF SLIDING PLATE (PROPOSED NAME)?

The FDA product code for MEDOFF SLIDING PLATE (PROPOSED NAME) is KTT.

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Related Devices (Code: KTT)

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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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