INS HILDEN TIBIAL ARZZT
FDA 510(k) clearance K133166 · decided 2014-11-06
Clearance details
- K-number
- K133166
- Device name
- INS HILDEN TIBIAL ARZZT
- Applicant
- Truemed Group, LLC
- Decision
- Substantially Equivalent
- Date received
- 2013-10-17
- Decision date
- 2014-11-06
- Days to decision
- 385 days
- Clearance type
- Traditional
- Product code
- HSB
- Device class
- 2
- Regulation number
- 888.3020
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Hampton, VA, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Truemed Group
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.