The following data is part of a premarket notification filed by Joint Medical Products Corp. with the FDA for S-rom Poly-dial Constrained Socket For Acet. Cup.
Device ID | K870271 |
510k Number | K870271 |
Device Name: | S-ROM POLY-DIAL CONSTRAINED SOCKET FOR ACET. CUP |
Classification | Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/polymer |
Applicant | JOINT MEDICAL PRODUCTS CORP. 1201 PENNSYLVANIA AVENUE, N.W. P.O. BOX 7566 Washington, DC 20044 |
Contact | Eugene I Lambert |
Correspondent | Eugene I Lambert JOINT MEDICAL PRODUCTS CORP. 1201 PENNSYLVANIA AVENUE, N.W. P.O. BOX 7566 Washington, DC 20044 |
Product Code | KWZ |
CFR Regulation Number | 888.3310 [🔎] |
Decision | Substantially Equivalent For Some Indications (SN) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-01-22 |
Decision Date | 1987-04-20 |