POREX(TM) MALAR IMPLANT
FDA 510(k) clearance K870182 · decided 1987-02-24
Clearance details
- K-number
- K870182
- Device name
- POREX(TM) MALAR IMPLANT
- Applicant
- Porex Medical
- Decision
- Substantially Equivalent
- Date received
- 1987-01-16
- Decision date
- 1987-02-24
- Days to decision
- 39 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Fairburn, GA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.