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FDA 510(k)

ORTHOMET ACETABULAR ROOF REINFORCEMENT RING

K-Number: K944856 · 1995-05-16

ApplicantWrightmedicaltechnologyinc
Decision Date1995-05-16
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ORTHOMET ACETABULAR ROOF REINFORCEMENT RING is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 1995-05-16 under 510(k) number K944856. 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 ORTHOMET ACETABULAR ROOF REINFORCEMENT RING?

ORTHOMET ACETABULAR ROOF REINFORCEMENT RING is a medical device that received FDA 510(k) clearance on 1995-05-16. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K944856.

When did ORTHOMET ACETABULAR ROOF REINFORCEMENT RING receive FDA 510(k) clearance?

ORTHOMET ACETABULAR ROOF REINFORCEMENT RING received FDA 510(k) clearance on 1995-05-16, under 510(k) number K944856.

Who is the listed applicant for ORTHOMET ACETABULAR ROOF REINFORCEMENT RING?

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 ORTHOMET ACETABULAR ROOF REINFORCEMENT RING?

The FDA product code for ORTHOMET ACETABULAR ROOF REINFORCEMENT RING 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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