HIPLOC COMPRESSION HIP SCREW— 510(k) K080685

Substantially Equivalent

Biomet Manufacturing, Inc.

FDA 510(k) clearance K080685 for HIPLOC COMPRESSION HIP SCREW, Substantially Equivalent on 2008-08-15. Applicant: Biomet Manufacturing, Inc.. Device class: 2.

Clearance details

Applicant
Biomet Manufacturing, Inc.
Product code
Code JDO
Device class
Class 2
Regulation
21 CFR 888.3030
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Warsaw, IN, US
Download summary PDFView on FDA.gov ↗

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Recalls naming K080685

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 K080685.

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