TRS CRANIAL BONE VOID FILLER(TRS C-BVF)— 510(k) K123633
Substantially EquivalentTissue Regeneration Systems, Inc.
FDA 510(k) clearance K123633 for TRS CRANIAL BONE VOID FILLER(TRS C-BVF), Substantially Equivalent on 2013-08-16. Applicant: Tissue Regeneration Systems, Inc.. Device class: 2.
Clearance details
- Applicant
- Tissue Regeneration Systems, Inc.
- Product code
- Code GXR
- Device class
- Class 2
- Regulation
- 21 CFR 882.5250
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Kirkland, WA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.