MEROGEL INJECTABLE BIORESORBABLE STENT— 510(k) K070886
Substantially EquivalentMedtronic, Inc.
FDA 510(k) clearance K070886 for MEROGEL INJECTABLE BIORESORBABLE STENT, Substantially Equivalent on 2007-04-26. Applicant: Medtronic, Inc.. Device class: 2.
Clearance details
- Applicant
- Medtronic, Inc.
- Product code
- Code NHB
- Device class
- Class 2
- Regulation
- 21 CFR 874.3620
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Jacksonville, FL, US
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