PERIOGRAF DURAPATITE 40-60 MESH— 510(k) K840260
Substantially EquivalentSterling Drug, Inc.
FDA 510(k) clearance K840260 for PERIOGRAF DURAPATITE 40-60 MESH, Substantially Equivalent on 1984-04-05. Applicant: Sterling Drug, Inc.. Device class: 2.
Clearance details
- Applicant
- Sterling Drug, Inc.
- Product code
- Code LYC
- Device class
- Class 2
- Regulation
- 21 CFR 872.3930
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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