AltiVate Anatomic Shoulder System— 510(k) K162024

Substantially Equivalent

Encore Medical L.P.

FDA 510(k) clearance K162024 for AltiVate Anatomic Shoulder System, Substantially Equivalent on 2016-11-21. Applicant: Encore Medical L.P.. Device class: 2.

Clearance details

Applicant
Encore Medical L.P.
Product code
Code KWS
Device class
Class 2
Regulation
21 CFR 888.3660
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Austin, TX, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code KWS

product code KWS
Death
6
Injury
9,652
Malfunction
1,385
Other
1
Total
11,044

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recalls naming K162024

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K162024.

Data sourced from openFDA. This site is unofficial and independent of the FDA.