Device Type ID | 4483 |
Device Name | Burr, Orthopedic |
Regulation Description | Orthopedic Manual Surgical Instrument. |
Regulation Medical Specialty | Orthopedic |
Review Panel | Orthopedic |
Premarket Review | Office Of Device Evaluation (ODE) Division Of Orthopedic Devices (DOD) Joint And Fixation Devices Branch Two ¿ Hips/Wrists/Fingers (JFDB2) |
Submission Type | 510(K) Exempt |
CFR Regulation Number | 888.4540 [🔎] |
FDA Device Classification | Class 1 Medical Device |
Product Code | HTT |
GMP Exempt | No |
Summary MR | Eligible |
Implanted Device | No |
Life Support Device | No |
Third Party Review | Not Third Party Eligible |
|
Device Type ID | 4483 |
Device | Burr, Orthopedic |
Product Code | HTT |
FDA Device Classification | Class 1 Medical Device |
Regulation Description | Orthopedic Manual Surgical Instrument. |
CFR Regulation Number | 888.4540 [🔎] |
Device Problems | |
---|---|
Break | 19 |
Detachment Of Device Component | 1 |
Fracture | 1 |
Device Operates Differently Than Expected | 1 |
Total Device Problems | 22 |
Recalls | |||
---|---|---|---|
Manufacturer | Recall Class | Date Posted | |
1 | The Anspach Effort, Inc. | II | May-09-2014 |
2 | Zimmer Gmbh | II | May-15-2017 |