SURGICAL CHISEL/OSTEOTOME— 510(k) K894785
Substantially EquivalentFdt Precision Machine Co., Inc.
FDA 510(k) clearance K894785 for SURGICAL CHISEL/OSTEOTOME, Substantially Equivalent on 1989-08-18. Applicant: Fdt Precision Machine Co., Inc.. Device class: 1.
Clearance details
- Applicant
- Fdt Precision Machine Co., 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
- Bridgeport, CT, US
Recent devices under product code KDG
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