CEDAR(TM) RETRACTOR RING
FDA 510(k) clearance K873691 · decided 1987-09-28
Clearance details
- K-number
- K873691
- Device name
- CEDAR(TM) RETRACTOR RING
- Applicant
- Cedar Surgical, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1987-09-08
- Decision date
- 1987-09-28
- Days to decision
- 20 days
- Clearance type
- Traditional
- Product code
- GZT
- Device class
- 2
- Regulation number
- 882.4800
- Medical specialty
- Neurology
- Advisory committee
- Neurology
- 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.