510(k) K951356
K951356 is an FDA 510(k) premarket notification submitted by Biologically Oriented Prostheses for the device "VARIOUS UHMWP HIP & KNEE JOINT PROSTHESIS MODIFIED". The FDA issued a decision of SN on June 19, 1995. The device falls under product code LPH (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented), a Class II device regulated under 21 CFR 888.3358. Biologically Oriented Prostheses has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SN ()
- Decision Date
- June 19, 1995
- Date Received
- March 24, 1995
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
- Device Class
- Class II
- Regulation Number
- 888.3358
- Review Panel
- OR
- Submission Type