OMC ORTHOMET CANNULATED SCREW
FDA 510(k) clearance K862157 · decided 1986-08-29
Clearance details
- K-number
- K862157
- Device name
- OMC ORTHOMET CANNULATED SCREW
- Applicant
- Orthomet, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1986-06-05
- Decision date
- 1986-08-29
- Days to decision
- 85 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Minneapolis, MN, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.