LIMACORPORATE SMR REVERSE SHOULDER SYSTEM
FDA 510(k) clearance K113523 · decided 2011-12-20
Clearance details
- K-number
- K113523
- Device name
- LIMACORPORATE SMR REVERSE SHOULDER SYSTEM
- Applicant
- Lima Corporate S.P.A.
- Decision
- Substantially Equivalent
- Date received
- 2011-11-29
- Decision date
- 2011-12-20
- Days to decision
- 21 days
- Clearance type
- Special
- Product code
- PHX
- Device class
- 2
- Regulation number
- 888.3660
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Winona Lake, IN, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Lima Corporate S.P.A.
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.