RAYLOR(TM) OSTEOTOMES
FDA 510(k) clearance K864423 · decided 1986-11-24
Clearance details
- K-number
- K864423
- Device name
- RAYLOR(TM) OSTEOTOMES
- Applicant
- Cedar Surgical, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1986-11-10
- Decision date
- 1986-11-24
- Days to decision
- 14 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Minnetonka, MN, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.