HEALIX ADVANCE SP PEEK Anchor
FDA 510(k) clearance K182941 · decided 2019-02-26
Clearance details
- K-number
- K182941
- Device name
- HEALIX ADVANCE SP PEEK Anchor
- Applicant
- Medos International SARL
- Decision
- Substantially Equivalent
- Date received
- 2018-10-23
- Decision date
- 2019-02-26
- Days to decision
- 126 days
- Clearance type
- Traditional
- Product code
- MBI
- Device class
- 2
- Regulation number
- 888.3040
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Le Locle, CH
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.