MODIFIED O.E.C. UNIV. SELF-ALIGNING ACETA. COMP.
FDA 510(k) clearance K884889 · decided 1989-02-27
Clearance details
- K-number
- K884889
- Device name
- MODIFIED O.E.C. UNIV. SELF-ALIGNING ACETA. COMP.
- Applicant
- Protek, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1988-11-22
- Decision date
- 1989-02-27
- Days to decision
- 97 days
- Clearance type
- Traditional
- Product code
- KWL
- Device class
- 2
- Regulation number
- 888.3360
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Indianapolis, IN, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.