Geister retractor for neuro - and spine surgery— 510(k) K180610
Substantially EquivalentGeister Medizin Technik GmbH
FDA 510(k) clearance K180610 for Geister retractor for neuro - and spine surgery, Substantially Equivalent on 2018-08-29. Applicant: Geister Medizin Technik GmbH. Device class: 2.
Clearance details
- Applicant
- Geister Medizin Technik GmbH
- Product code
- Code GZT
- Device class
- Class 2
- Regulation
- 21 CFR 882.4800
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tuttlingen, DE
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Data sourced from openFDA. This site is unofficial and independent of the FDA.