SPINEOLOGY FACET SCREW— 510(k) K092464

Substantially Equivalent

Spineology, Inc.

FDA 510(k) clearance K092464 for SPINEOLOGY FACET SCREW, Substantially Equivalent on 2009-11-09. Applicant: Spineology, Inc.. Device class: Unclassified.

Clearance details

Applicant
Spineology, Inc.
Product code
Code MRW
Device class
Unclassified
Advisory panel
Unknown
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
St. Paul, MN, US
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