OSTEOVATION CMF BONE VOID FILLER— 510(k) K051784

Substantially Equivalent

Skeletal Kinetics, LLC

FDA 510(k) clearance K051784 for OSTEOVATION CMF BONE VOID FILLER, Substantially Equivalent on 2005-07-20. Applicant: Skeletal Kinetics, LLC. Device class: 2.

Clearance details

Applicant
Skeletal Kinetics, LLC
Product code
Code GXP
Device class
Class 2
Regulation
21 CFR 882.5300
Advisory panel
Neurology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Cupertino, CA, US
Download summary PDFView on FDA.gov ↗

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Recalls naming K051784

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 K051784.

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