510(k) K831712
- Device
- SURGICAL DRILL BITS
- Applicant
- MEDICAL SPECIALISTS IN PACKAGING
- 510(k) number
- K831712
- Product code
- HTW
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1983-07-07
- Date received
- 1983-05-27
- Regulation
- 888.4540
- Classification name
- Bit, Drill
- Medical specialty
- Orthopedic
- Review panel
- Orthopedic
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 3015974593
- 3012755988
- 3010687973
- 3007143290
- 1722511
- 3004475955
- 3010160527
- 3009882675
- 1835572
- 3015451162
- 3004549189
- 3009141957
- 1043534
- 3014004349
- 3042285592
- 3014938863
- 3011530718
- 3014967149
- 8043862
- 1051526
- 1421879
- 3006017180
- 3011024991
- 3009590742
- 3012818475
- 3030412764
- 3030514683
- 3023265483
- 1223421
- 3011577940
- 3003418325
- 3017823294
- 3003431869
- 3013700547
- 8030607
- 3011600579
- 3007539489
- 3002808227
- 3015877656
- 3015151147
- 3010370500
- 3008902714
- 3006950086
- 8010300
- 3008323540
- 3002806535
- 3006460162
- 3010388970
- 3004431266
- 3006982954
- 3013055499
- 3013875765
- 2183449
- 2649614
- 3013011598
- 3007441485
- 3007319107
- 9613350
- 3012329926
- 9615765
- 3011874600
- 3015831087
- 3021948057
- 3006395932
- 8023007
- 3005575604
- 3006563559
- 3002834291
- 9616944
- 3007700286
- 3014554088
- 3003249380
- 3009165919
- 1220246
- 1038671
- 3012536737
- 9611102
- 1720929
- 1526534
- 3001620590
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code HTW #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K151661 | Renovo Life Hard Carbon Coated Drill Bit | Renovo Life, LLC | 2016-01-15 |
| K942906 | AGEE-WRISTJACK PRE-DRILL KIT | Hand Biomechanics Lab, Inc. | 1994-12-22 |
| K930339 | REAMER BIT | Neoligaments, Ltd. | 1993-08-06 |
| K915692 | CANNULATED DRILL BIT | W. L. Gore & Associates, Inc. | 1992-01-16 |
| K892903 | MITEK ANCHOR DRILL | Mitek Surgical Products, Inc. | 1989-10-06 |
| K870217 | FEMORAL CEMENT REMOVAL INSTRUMENTS | Kenneth J. Hoek, M.D., Inc. | 1987-02-06 |
| K863147 | GLENOID DRILL | Bowen & Company, Inc. | 1986-09-05 |
| K841629 | DRILL BIT | Plastafil, Inc. | 1984-08-27 |
| K834229 | BONE PLUGGING TOOL | Standard Surgical | 1984-01-10 |
| K820226 | UNIVERSALL DRILL GUIDE | Ortho Pared Instruments, Inc. | 1982-02-04 |
Legacy Summary#
Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases
FDA Review#
Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases