The following data is part of a premarket notification filed by Ortho Development Corp. with the FDA for Headloc Ceramic Head.
Device ID | K971426 |
510k Number | K971426 |
Device Name: | HEADLOC CERAMIC HEAD |
Classification | Prosthesis, Hip, Semi-constrained, Metal/ceramic/polymer, Cemented Or Non-porous, Uncemented |
Applicant | ORTHO DEVELOPMENT CORP. 106 WEST 12200 SOUTH Draper, UT 84020 |
Contact | Carol J Freasier |
Correspondent | Carol J Freasier ORTHO DEVELOPMENT CORP. 106 WEST 12200 SOUTH Draper, UT 84020 |
Product Code | LZO |
CFR Regulation Number | 888.3353 [🔎] |
Decision | Substantially Equivalent For Some Indications (SN) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-04-17 |
Decision Date | 1997-07-09 |