ANSPACH MENISECTOMY KNIFE— 510(k) K803178
Substantially EquivalentThe Anspach Effort, Inc.
FDA 510(k) clearance K803178 for ANSPACH MENISECTOMY KNIFE, Substantially Equivalent on 1981-02-13. Applicant: The Anspach Effort, Inc.. Device class: 1.
Clearance details
- Applicant
- The Anspach Effort, Inc.
- Product code
- Code FZS
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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