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FDA 510(k)

Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System

K-Number: K260102 · 2026-06-12

ApplicantStryker Corporation (Tornier, Inc.)
Decision Date2026-06-12
Product CodePHX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corporation (Tornier, Inc.). It received FDA 510(k) clearance on 2026-06-12 under 510(k) number K260102. 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 Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System?

Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System is a medical device that received FDA 510(k) clearance on 2026-06-12. The listed applicant is Stryker Corporation (Tornier, Inc.). The 510(k) number is K260102.

When did Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System receive FDA 510(k) clearance?

Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System received FDA 510(k) clearance on 2026-06-12, under 510(k) number K260102.

Who is the listed applicant for Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System?

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

What is the FDA product code for Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System?

The FDA product code for Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System is PHX.

Related Clinical Trials

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.

NCT03726554Post-Market Study of Comprehensive Reverse Augmented Glenoid and Mini Humeral Tray in Total Shoulder ArthroplastyACTIVE_NOT_RECRUITINGNCT05500066Tornier HRS (Humeral Reconstruction System) Study (REVIVE)ENROLLING_BY_INVITATION

Other records listing Stryker Corporation (Tornier, Inc.) as applicant

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.

K241878Tornier Humeral Reconstruction System (Tornier HRS); Tornier Perform Humeral System - Stem (Tornier PHS-Stem)K241609Tornier Humeral Reconstruction System (Tornier HRS)

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.K261016MSS - Humeral reverse liners extensionMedacta International, SAK253992Veritas Reverse Total Shoulder SystemRestor3DK252404Comprehensive Reverse Shoulder - HA Glenosphere BaseplatesBiomet OrthopedicsK260583Equinoxe® Shoulder SystemExactech, Inc.

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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