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FDA 510(k)

ASCEND SHOULDER SYSTEM

K-Number: K120794 · 2012-04-13

ApplicantTornier, Inc.
Decision Date2012-04-13
Product CodeKWS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ASCEND SHOULDER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Tornier, Inc.. It received FDA 510(k) clearance on 2012-04-13 under 510(k) number K120794. The device is classified under product code KWS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASCEND SHOULDER SYSTEM?

ASCEND SHOULDER SYSTEM is a medical device that received FDA 510(k) clearance on 2012-04-13. The listed applicant is Tornier, Inc.. The 510(k) number is K120794.

When did ASCEND SHOULDER SYSTEM receive FDA 510(k) clearance?

ASCEND SHOULDER SYSTEM received FDA 510(k) clearance on 2012-04-13, under 510(k) number K120794.

Who is the listed applicant for ASCEND SHOULDER SYSTEM?

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

What is the FDA product code for ASCEND SHOULDER SYSTEM?

The FDA product code for ASCEND SHOULDER SYSTEM is KWS.

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.

Other records listing 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.

View all 46 devices →

Related Devices (Code: KWS)

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.

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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