Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Joint Medical Products Corp. · Predicate Candidate Screening
33 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
147 daysmedian FDA review time
346 days90th percentile
33clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K955511 | ARTHOPOR I & II ACETABULAR CUP/ARTHOPOR II OBLONG ACETABULAR | Joint Medical Products Corp. | 1996-02-26 | 84 | 0 |
| K954935 | S-ROM FEMORAL HIP STEM - SIZE 14 X 8 | Joint Medical Products Corp. | 1996-01-22 | 87 | 0 |
| K944321 | S-ROM NOILES POSTERIOR STABILIZED TOTAL KNEE SYSTEM II | Joint Medical Products Corp. | 1995-08-14 | 346 | 0 |
| K951726 | S-ROM ZTP UHMWPE ACETABULAR CUP | Joint Medical Products Corp. | 1995-06-21 | 68 | 0 |
| K951084 | S-ROM OPC (ONE-PIECE CEMENTED) II FEMORAL HIP PROSTHESIS | Joint Medical Products Corp. | 1995-05-31 | 83 | 0 |
| K951000 | ZTT I AND II ACETABULAR CUP OF THE S-ROM TOTAL HIP SYSTEM | Joint Medical Products Corp. | 1995-04-14 | 42 | 0 |
| K941769 | KNEE PROTHESIS | Joint Medical Products Corp. | 1995-02-01 | 296 | 0 |
| K936037 | S-ROM NOILES CRUCIATE RETAINING KNEE | Joint Medical Products Corp. | 1994-10-03 | 287 | 0 |
| K934412 | COATED ZT PROXIMAL SLEEVE | Joint Medical Products Corp. | 1994-06-03 | 266 | 0 |
| K931676 | S-ROM(R) ZTT(TM) ACETABULAR CUP-APICAL HOLE PLUG | Joint Medical Products Corp. | 1994-05-18 | 407 | 0 |
| K935078 | S-ROM TOTAL HIP REPLACEMENT SYSTEM | Joint Medical Products Corp. | 1994-03-09 | 135 | 0 |
| K924940 | FEMORAL & TIBIAL AUGMENT BLOCK | Joint Medical Products Corp. | 1993-03-09 | 160 | 0 |
| K920739 | S-ROM TOTAL HIP REPLACEMENT SYSTEM | Joint Medical Products Corp. | 1992-11-24 | 279 | 0 |
| K924492 | POLY-DIAL INSERTS | Joint Medical Products Corp. | 1992-11-24 | 82 | 0 |
| K921111 | S-ROM ZIRCONIA CERMAMIC FEMORAL HEAD | Joint Medical Products Corp. | 1992-10-22 | 227 | 0 |
| K922824 | KNEE JT. PATELLO FEMORO TIBIAL POLYMER/METAL/POLYM | Joint Medical Products Corp. | 1992-09-17 | 98 | 0 |
| K920317 | S-ROM LF FEMORAL HEAD | Joint Medical Products Corp. | 1992-03-19 | 55 | 0 |
| K912713 | S-ROM ZT HA PROXIMAL FEMORAL SLEEVE | Joint Medical Products Corp. | 1991-12-30 | 193 | 0 |
| K913231 | S-ROM(TM) TOTAL LHIP SYSTEM W/CERAMIC HEAD | Joint Medical Products Corp. | 1991-12-20 | 151 | 0 |
| K905810 | NOILES(TM) TOTAL KNEE PROSTHESIS, MODIFICATION | Joint Medical Products Corp. | 1991-06-12 | 168 | 0 |
| K905258 | S-ROM OBLONG ACETABULAR CUP | Joint Medical Products Corp. | 1991-05-21 | 181 | 0 |
| K904746 | S-ROM(TM) FEMORAL STEM CENTRALIZER/CEMENT SPACER | Joint Medical Products Corp. | 1990-11-20 | 33 | 0 |
| K896048 | S-ROM/NOILES MARK 3 | Joint Medical Products Corp. | 1990-03-14 | 147 | 6 |
| K896397 | S-ROM(TM)/NOILES(TM) MARK 5 KNEE | Joint Medical Products Corp. | 1990-02-22 | 107 | 0 |
| K893584 | GRIPPER II ACETABULAR CUP | Joint Medical Products Corp. | 1989-07-28 | 80 | 0 |
| K870088 | S-ROM SUPERCUP ACETABULAR CUP | Joint Medical Products Corp. | 1988-04-22 | 469 | 0 |
| K870730 | NOILES TOTAL KNEE PROSTHESIS | Joint Medical Products Corp. | 1987-05-26 | 90 | 0 |
| K870271 | S-ROM POLY-DIAL CONSTRAINED SOCKET FOR ACET. CUP | Joint Medical Products Corp. | 1987-04-20 | 88 | 0 |
| K860207 | S-ROM 135 POROUS COATED FEMORAL STEM COLLAR | Joint Medical Products Corp. | 1986-08-06 | 196 | 0 |
| K844050 | ARTHOPOR-ACETABULAR COMPONENT | Joint Medical Products Corp. | 1985-12-06 | 415 | 0 |
| K851422 | S-ROM 135 FEMORAL STEM & COLLAR(PART OF S-ROM HIP | Joint Medical Products Corp. | 1985-09-18 | 161 | 0 |
| K851421 | S-ROM ACETABULAR CUP(PART OF S-ROM 135TM TOTAL HIP | Joint Medical Products Corp. | 1985-06-04 | 55 | 0 |
| K841022 | SRC TOTAL KNEE | Joint Medical Products Corp. | 1984-06-25 | 105 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda