STRYKER SPINE OASYS BONE SCREW— 510(k) K031657
Substantially EquivalentHowmedica Osteonics Corp.
FDA 510(k) clearance K031657 for STRYKER SPINE OASYS BONE SCREW, Substantially Equivalent on 2003-08-22. Applicant: Howmedica Osteonics Corp.. Device class: Unclassified.
Clearance details
- Applicant
- Howmedica Osteonics Corp.
- Product code
- Code MRW
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Allendale, NJ, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.