510(k) K111232
K111232 is an FDA 510(k) premarket notification submitted by Pega Medical, Inc. for the device "GAP ENDO-EXO MEDULLARY SYSTEM". The FDA issued a decision of Substantially Equivalent on January 26, 2012. The device falls under product code HSB (Rod, Fixation, Intramedullary And Accessories), a Class II device regulated under 21 CFR 888.3020. Pega Medical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 26, 2012
- Date Received
- May 2, 2011
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Rod, Fixation, Intramedullary And Accessories
- Device Class
- Class II
- Regulation Number
- 888.3020
- Review Panel
- OR
- Submission Type