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FDA 510(k)

LETOURNEL ACETABULAR PLATE

K-Number: K850401 · 1985-04-19

ApplicantPfizer, Inc.
Decision Date1985-04-19
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LETOURNEL ACETABULAR PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Pfizer, Inc.. It received FDA 510(k) clearance on 1985-04-19 under 510(k) number K850401. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LETOURNEL ACETABULAR PLATE?

LETOURNEL ACETABULAR PLATE is a medical device that received FDA 510(k) clearance on 1985-04-19. The listed applicant is Pfizer, Inc.. The 510(k) number is K850401.

When did LETOURNEL ACETABULAR PLATE receive FDA 510(k) clearance?

LETOURNEL ACETABULAR PLATE received FDA 510(k) clearance on 1985-04-19, under 510(k) number K850401.

Who is the listed applicant for LETOURNEL ACETABULAR PLATE?

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

What is the FDA product code for LETOURNEL ACETABULAR PLATE?

The FDA product code for LETOURNEL ACETABULAR PLATE is HRS.

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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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