Screw 6302-3-022
GUDID 07613327036237
Bone Screw - Hex Drive Selftap
Howmedica Osteonics Corp.
Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding)| Primary Device ID | 07613327036237 |
| NIH Device Record Key | 8364f371-fb87-4014-b80a-34f27618d237 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Screw |
| Version Model Number | 6302-3-022 |
| Catalog Number | 6302-3-022 |
| Company DUNS | 058311945 |
| Company Name | Howmedica Osteonics Corp. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Device Dimensions
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
| Device Size Text, specify | 0 |
| Length | 22 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327036237 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K933102
FDA Product Code
| LPH | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-09-24 |
On-Brand Devices [Screw]
| 07613327036961 | Cancellous Bone Screw |
| 07613327036954 | Cancellous Bone Screw |
| 07613327036947 | Cancellous Bone Screw |
| 07613327036930 | Cancellous Bone Screw |
| 07613327036923 | Cancellous Bone Screw |
| 07613327036916 | Cancellous Bone Screw |
| 07613327036909 | Cancellous Bone Screw |
| 07613327036893 | Cancellous Bone Screw |
| 07613327036886 | Cancellous Bone Screw |
| 07613327036879 | Cancellous Bone Screw |
| 07613327036862 | Cancellous Bone Screw |
| 07613327036855 | Cancellous Bone Screw |
| 07613327036848 | Cancellous Bone Screw |
| 07613327036831 | Cancellous Bone Screw |
| 07613327036824 | Cancellous Bone Screw |
| 07613327036817 | Cancellous Bone Screw |
| 07613327036800 | Cancellous Bone Screw |
| 07613327036794 | Cancellous Bone Screw |
| 07613327036787 | Cancellous Bone Screw |
| 07613327036770 | Cancellous Bone Screw |
| 07613327036763 | Cancellous Bone Screw |
| 07613327036756 | Cancellous Bone Screw |
| 07613327036749 | Cancellous Bone Screw |
| 07613327036732 | Cancellous Bone Screw |
| 07613327036725 | Cancellous Bone Screw |
| 07613327036718 | Cancellous Bone Screw |
| 07613327036701 | Cancellous Bone Screw |
| 07613327036688 | Cancellous Bone Screw |
| 07613327036312 | Bone Screw - Hex Drive Selftap |
| 07613327036305 | Bone Screw - Hex Drive Selftap |
| 07613327036299 | Bone Screw - Hex Drive Selftap |
| 07613327036282 | Bone Screw - Hex Drive Selftap |
| 07613327036275 | Bone Screw - Hex Drive Selftap |
| 07613327036268 | Bone Screw - Hex Drive Selftap |
| 07613327036251 | Bone Screw - Hex Drive Selftap |
| 07613327036244 | Bone Screw - Hex Drive Selftap |
| 07613327036237 | Bone Screw - Hex Drive Selftap |
| 07613327036220 | Bone Screw - Hex Drive Selftap |
| 07613327036213 | Bone Screw - Hex Drive Selftap |
| 07613327036206 | Bone Screw - Hex Drive Selftap |
| 07613327036190 | Bone Screw - Hex Drive Selftap |
| 07613327036183 | Bone Screw - Hex Drive Selftap |
| 07613327036169 | Hex Drive Self-Tapping Bone Screw |
| 07613327036152 | Hex Drive Self-Tapping Bone Screw |
| 07613327036145 | Hex Drive Self-Tapping Bone Screw |
| 07613327036138 | Hex Drive Self-Tapping Screw |
| 07613327036121 | Hex Drive Self-Tapping Screw |
| 07613327036114 | Hex Drive Self-Tapping Screw |
| 07613327036107 | Hex Drive Self-Tapping Screw |
| 07613327036091 | Hex Drive Self-Tapping Screw |
Trademark Results [Screw]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SCREW 97057329 not registered Live/Pending |
Wasserman, Heath, Norman 2021-10-02 |
 SCREW 88006262 not registered Dead/Abandoned |
Wasserman Heath Norman 2018-06-19 |
 SCREW 87735536 5667439 Live/Registered |
Coonan, John 2017-12-27 |
 SCREW 85010060 not registered Dead/Abandoned |
Squiers, Phil 2010-04-09 |
 SCREW 78812505 3311938 Dead/Cancelled |
VISSAGE PRODUCTIONS LLC 2006-02-10 |
 SCREW 77784088 not registered Dead/Abandoned |
TUTM Entertainment, Inc. 2009-07-17 |
 SCREW 76598834 3221029 Live/Registered |
Stratus Vineyards Limited 2004-06-23 |
 SCREW 76557086 not registered Dead/Abandoned |
SCREWED UP ENTERTAINMENT, INC 2003-10-08 |
 SCREW 76446431 not registered Dead/Abandoned |
Hof, Dennis 2002-09-03 |
 SCREW 75650819 not registered Dead/Abandoned |
BC&C APPAREL, INC. 1999-02-26 |
SCREW 75650819 not registered Dead/Abandoned |
Bynum, W. Blaine 1999-02-26 |
 SCREW 75537772 not registered Dead/Abandoned |
Goldstein, Al 1998-08-17 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.