EXETER MESH— 510(k) K963940
Substantially EquivalentHowmedica, Inc.
FDA 510(k) clearance K963940 for EXETER MESH, Substantially Equivalent on 1997-02-13. Applicant: Howmedica, Inc.. Device class: 2.
Clearance details
- Applicant
- Howmedica, Inc.
- Product code
- Code JDJ
- Device class
- Class 2
- Regulation
- 21 CFR 878.3300
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Rutherford, NJ, US
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