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FDA 510(k)

MAXIM RPG PS FEMORAL COMPONENT

K-Number: K012348 · 2001-08-15

ApplicantBiomet, Inc.
Decision Date2001-08-15
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MAXIM RPG PS FEMORAL COMPONENT is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2001-08-15 under 510(k) number K012348. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAXIM RPG PS FEMORAL COMPONENT?

MAXIM RPG PS FEMORAL COMPONENT is a medical device that received FDA 510(k) clearance on 2001-08-15. The listed applicant is Biomet, Inc.. The 510(k) number is K012348.

When did MAXIM RPG PS FEMORAL COMPONENT receive FDA 510(k) clearance?

MAXIM RPG PS FEMORAL COMPONENT received FDA 510(k) clearance on 2001-08-15, under 510(k) number K012348.

Who is the listed applicant for MAXIM RPG PS FEMORAL COMPONENT?

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

What is the FDA product code for MAXIM RPG PS FEMORAL COMPONENT?

The FDA product code for MAXIM RPG PS FEMORAL COMPONENT is JWH.

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Other records listing Biomet, Inc. as applicant

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Related Devices (Code: JWH)

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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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