K954800Substantially Equivalent for Some Indications
Apr Hip Sys W/cal-Coated Can Str Titanium (Csti)
Intermedics Orthopedics, Austin TX / Traditional, Substantially Equivalent for Some Indications
K954800 is the FDA 510(k) clearance record for APR HIP SYS W/CAL-COATED CAN STR TITANIUM (CSTI), a class II device, cleared for Intermedics Orthopedics on under FDA product code MEH (Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate). FDA records list 108 510(k) clearances for Intermedics Orthopedics, from to . As of , FDA records show one recall naming K954800.
Clearance record
- Decision date
- Received
- (211 days to decision)
- Product code
- MEH Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate
- Regulation
- 21 CFR 888.3353
- Device class
- Class II
- Review panel
- Orthopedic
- Applicant
- Intermedics Orthopedics 9900 Spectrum Dr., Austin TX
- Third party review
- No
Clearances, product code MEH
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 1 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 1 |
| September 2026 | 0 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
