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FDA 510(k)

COMPREHENSIVE REVERSE SHOULDER

K-Number: K080642 · 2008-07-09

ApplicantBiomet, Inc.
Decision Date2008-07-09
Product CodePHX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

COMPREHENSIVE REVERSE SHOULDER is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2008-07-09 under 510(k) number K080642. The device is classified under product code PHX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPREHENSIVE REVERSE SHOULDER?

COMPREHENSIVE REVERSE SHOULDER is a medical device that received FDA 510(k) clearance on 2008-07-09. The listed applicant is Biomet, Inc.. The 510(k) number is K080642.

When did COMPREHENSIVE REVERSE SHOULDER receive FDA 510(k) clearance?

COMPREHENSIVE REVERSE SHOULDER received FDA 510(k) clearance on 2008-07-09, under 510(k) number K080642.

Who is the listed applicant for COMPREHENSIVE REVERSE SHOULDER?

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 COMPREHENSIVE REVERSE SHOULDER?

The FDA product code for COMPREHENSIVE REVERSE SHOULDER is PHX.

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Other records listing Biomet, Inc. as applicant

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Related Devices (Code: PHX)

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.

K260556Veritas Shoulder SystemRestor3DK261683Augment Off-Axis Instrument SystemZimmer, Inc.K260102Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder SystemStryker Corporation (Tornier, Inc.)K261016MSS - Humeral reverse liners extensionMedacta International, SAK253992Veritas Reverse Total Shoulder SystemRestor3DK252404Comprehensive Reverse Shoulder - HA Glenosphere BaseplatesBiomet Orthopedics

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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