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FDA 510(k)

BI-ANGULAR SHOULDER SYSTEM

K-Number: K032895 · 2003-11-20

ApplicantBiomet, Inc.
Decision Date2003-11-20
Product CodeMBF
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BI-ANGULAR SHOULDER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2003-11-20 under 510(k) number K032895. The device is classified under product code MBF. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BI-ANGULAR SHOULDER SYSTEM?

BI-ANGULAR SHOULDER SYSTEM is a medical device that received FDA 510(k) clearance on 2003-11-20. The listed applicant is Biomet, Inc.. The 510(k) number is K032895.

When did BI-ANGULAR SHOULDER SYSTEM receive FDA 510(k) clearance?

BI-ANGULAR SHOULDER SYSTEM received FDA 510(k) clearance on 2003-11-20, under 510(k) number K032895.

Who is the listed applicant for BI-ANGULAR SHOULDER SYSTEM?

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 BI-ANGULAR SHOULDER SYSTEM?

The FDA product code for BI-ANGULAR SHOULDER SYSTEM is MBF.

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Other records listing Biomet, Inc. as applicant

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Related Devices (Code: MBF)

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.

K253592Zimmer Biomet Reverse Shoulder Prosthesis (Alliance Humeral Bearings, Identity Humeral Trays, Comprehensive Reverse Humeral Trays, Comprehensive Reverse 32mm Glenospheres and Adapter)Zimmer, Inc.K251098Identity Revision Humeral StemsZimmer, Inc.K250848Identity Shoulder SystemZimmer, Inc.K240876Identity Shoulder SystemZimmer, Inc.K233712PRIMA Humeral System; PRIMA TT GlenoidLima Corporate S.P.A.K231099SMR Hybrid Glenoid SystemLima Corporate S.P.A.

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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