SILVER OSTEOTOME— 510(k) K772374
Substantially EquivalentEdward Weck, Inc.
FDA 510(k) clearance K772374 for SILVER OSTEOTOME, Substantially Equivalent on 1978-03-09. Applicant: Edward Weck, Inc.. Device class: 1.
Clearance details
- Applicant
- Edward Weck, Inc.
- Product code
- Code KDG
- Device class
- Class 1
- Regulation
- 21 CFR 878.4820
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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