Integrity Implant— 510(k) K223538
Substantially EquivalentAnika Therapeutics, Inc.
FDA 510(k) clearance K223538 for Integrity Implant, Substantially Equivalent on 2023-08-17. Applicant: Anika Therapeutics, Inc.. Device class: 2.
Clearance details
- Applicant
- Anika Therapeutics, Inc.
- Product code
- Code OWX
- 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
- Beford, MA, US
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