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FDA 510(k)

PELVIC RADIUS PLATE

K-Number: K936233 · 1994-08-01

ApplicantSmith & Nephew Richards, Inc.
Decision Date1994-08-01
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PELVIC RADIUS PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew Richards, Inc.. It received FDA 510(k) clearance on 1994-08-01 under 510(k) number K936233. 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 PELVIC RADIUS PLATE?

PELVIC RADIUS PLATE is a medical device that received FDA 510(k) clearance on 1994-08-01. The listed applicant is Smith & Nephew Richards, Inc.. The 510(k) number is K936233.

When did PELVIC RADIUS PLATE receive FDA 510(k) clearance?

PELVIC RADIUS PLATE received FDA 510(k) clearance on 1994-08-01, under 510(k) number K936233.

Who is the listed applicant for PELVIC RADIUS PLATE?

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

What is the FDA product code for PELVIC RADIUS PLATE?

The FDA product code for PELVIC RADIUS PLATE is HRS.

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Other records listing Smith & Nephew Richards, Inc. as applicant

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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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