Xia® Growth Rod Conversion Set— 510(k) K142114
Substantially EquivalentStryker Corporation
FDA 510(k) clearance K142114 for Xia® Growth Rod Conversion Set, Substantially Equivalent on 2014-10-27. Applicant: Stryker Corporation. Device class: 2.
Clearance details
- Applicant
- Stryker Corporation
- Product code
- Code PGM
- Device class
- Class 2
- Regulation
- 21 CFR 888.3070
- Advisory panel
- Orthopedic
- 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.