RESIDUAL LIMB LENGTHENING SYSTEM— 510(k) K141739

Substantially Equivalent

Ellipse Technologies, Inc.

FDA 510(k) clearance K141739 for RESIDUAL LIMB LENGTHENING SYSTEM, Substantially Equivalent on 2014-10-07. Applicant: Ellipse Technologies, Inc.. Device class: 2.

Clearance details

Applicant
Ellipse Technologies, Inc.
Product code
Code HSB
Device class
Class 2
Regulation
21 CFR 888.3020
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Irvine, CA, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code HSB

product code HSB
Death
49
Injury
12,083
Malfunction
6,561
Other
1
Total
18,694

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 K141739

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 K141739.

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