MEDPOR PLUS SURGICAL IMPLANT BIOMATERIAL— 510(k) K012350
Substantially EquivalentPorex Surgical, Inc.
FDA 510(k) clearance K012350 for MEDPOR PLUS SURGICAL IMPLANT BIOMATERIAL, Substantially Equivalent on 2002-03-14. Applicant: Porex Surgical, Inc.. Device class: 2.
Clearance details
- Applicant
- Porex Surgical, Inc.
- Product code
- Code FWP
- Device class
- Class 2
- Regulation
- 21 CFR 878.3550
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Newnan, GA, US
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