FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MEROGEL INJECTABLE BIORESORBABLE STENT
K Number: K070886
·
Decision Apr 26, 2007
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
14
Applicant Total
209
Review Days
27
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Basic Information
- Device Name
- MEROGEL INJECTABLE BIORESORBABLE STENT
- K Number
- K070886
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 874.3620
- Medical Specialty
- Ear, Nose, Throat
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Medtronic, Inc.
- Date Received
- March 30, 2007
- Decision Date
- April 26, 2007
- Product Code
- NHB
- Advisory Committee
- Ear, Nose, Throat
- Review Advisory Committee
- EN
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| NHB | Polymer, Ear, Nose And Throat, Synthetic, Absorbable | FDA class 2 | Ear, Nose, Throat |
Similar 510(k) Clearances
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