MITEK DRILL GUIDE— 510(k) K892904
Substantially EquivalentMitek Surgical Products, Inc.
FDA 510(k) clearance K892904 for MITEK DRILL GUIDE, Substantially Equivalent on 1989-09-28. Applicant: Mitek Surgical Products, Inc.. Device class: 1.
Clearance details
- Applicant
- Mitek Surgical Products, Inc.
- Product code
- Code HXY
- Device class
- Class 1
- Regulation
- 21 CFR 888.4540
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Dedham, MA, US
Recent devices under product code HXY
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