STRYKER CMF MEDPOR CUSTOMIZED IMPLANT— 510(k) K121315
Substantially EquivalentHowmedica Osteonics Corp.
FDA 510(k) clearance K121315 for STRYKER CMF MEDPOR CUSTOMIZED IMPLANT, Substantially Equivalent on 2012-11-01. Applicant: Howmedica Osteonics Corp.. Device class: 2.
Clearance details
- Applicant
- Howmedica Osteonics Corp.
- Product code
- Code FWP
- Device class
- Class 2
- Regulation
- 21 CFR 878.3550
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Newnan, GA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.