BONE ANCHOR SYSTEM III (BAS III)
FDA 510(k) clearance K990295 · decided 1999-03-05
Clearance details
- K-number
- K990295
- Device name
- BONE ANCHOR SYSTEM III (BAS III)
- Applicant
- Boston Scientific Corp
- Decision
- Substantially Equivalent
- Date received
- 1999-01-29
- Decision date
- 1999-03-05
- Days to decision
- 35 days
- Clearance type
- Traditional
- Product code
- MBI
- Device class
- 2
- Regulation number
- 888.3040
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Natick,, MA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.