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FDA 510(k)

VANGUARD CR STEM HOUSINGS

K-Number: K082826 · 2008-10-24

ApplicantBiomet Manufacturing Corp
Decision Date2008-10-24
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VANGUARD CR STEM HOUSINGS is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Manufacturing Corp. It received FDA 510(k) clearance on 2008-10-24 under 510(k) number K082826. 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 VANGUARD CR STEM HOUSINGS?

VANGUARD CR STEM HOUSINGS is a medical device that received FDA 510(k) clearance on 2008-10-24. The listed applicant is Biomet Manufacturing Corp. The 510(k) number is K082826.

When did VANGUARD CR STEM HOUSINGS receive FDA 510(k) clearance?

VANGUARD CR STEM HOUSINGS received FDA 510(k) clearance on 2008-10-24, under 510(k) number K082826.

Who is the listed applicant for VANGUARD CR STEM HOUSINGS?

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

What is the FDA product code for VANGUARD CR STEM HOUSINGS?

The FDA product code for VANGUARD CR STEM HOUSINGS is 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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