HALL ARTHROTOME
FDA 510(k) clearance K832816 · decided 1983-11-28
Clearance details
- K-number
- K832816
- Device name
- HALL ARTHROTOME
- Applicant
- American Sterilizer Co.
- Decision
- Substantially Equivalent
- Date received
- 1983-08-19
- Decision date
- 1983-11-28
- Days to decision
- 101 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Walker, MI, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.