S2 POSTERIOR-TIB— 510(k) K832296
Substantially EquivalentAnstek Corp.
FDA 510(k) clearance K832296 for S2 POSTERIOR-TIB, Substantially Equivalent on 1983-08-31. Applicant: Anstek Corp.. Device class: 2.
Clearance details
- Applicant
- Anstek Corp.
- Product code
- Code GXY
- Device class
- Class 2
- Regulation
- 21 CFR 882.1320
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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view allData sourced from openFDA. This site is unofficial and independent of the FDA.